جستجوی مقالات مرتبط با کلیدواژه « Tumors » در نشریات گروه « پزشکی »
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Background
Eyelid tumors are common in the daily practice of skin tumors and are composed of benign and malignant lesions.
MethodsThis retrospective case series study collected histopathologic reports of eyelid tumors of patients treated between 2022 and 2023 in Razi and Farabi hospitals (Tehran, Iran). Patient data, including patient age, sex, location of the lesion, and recurrence, were collected. Descriptive and inferential statistics were used to characterize the subgroups.
ResultsThe sample was composed of 154 eyelid tumor specimens, including 72 (47%) malignant cases, 80 (52%) benign cases, and 2 (1%) premalignant cases. Malignant tumors included 81.9% basal cell carcinomas (BCC), 15.3% basosquamous cell carcinomas (BSC), and 1.4% squamous cell carcinoma (SCC). The benign eyelid lesions were comprised of 20% intradermal melanocytic nevus, 11.3% epidermal cyst, 7.6% dermoid cyst, 10% seborrheic keratosis, 6.3% xanthelasma, 2.5% wart, 3.8% compound nevus, 5% fibroconnective tissue, 3.8% squamous papilloma, 3.8% neurofibroma, 2.5% comedone,2.5% apocrine hidrocystoma, 2.5% foreign body type granuloma, and 1.3% of others (arteriovenous hemangioma, cavernous hemangioma, cutaneous horn, etc.) The premalignant lesions were 2 cases of actinic keratosis. Benign lesions had an equal frequency of occurrence in the upper and lower lids. Malignant lesions were seen more in the lower lid. Premalignant lesions were seen in the lower lid. The mean age at diagnosis was 45.8 ± 23.06 years for patients with benign lesions and 63.5 ± 16.7 years for patients with malignant lesions. The mean age for patients with premalignant lesions was 81.5 ± 9.19 years (P < 0.001).
ConclusionsIn our study, benign lesions were seen predominantly in young persons and malignant lesions were mostly seen in elderly persons. There is an equal occurrence of malignant lesions in males and females, and recurrence after excision was infrequent.
Keywords: Eyelids, Malignant, Benign, Tumors, Basal Cell Carcinoma, Basosquamous Cell Carcinoma} -
مقدمه
غده پینه آل یک غده درون ریز کوچک به شکل کاج است که در تنظیم بیولوژیکی ریتم شبانه روزی موثر میباشد. تومورهای ناحیه پینه آل تقریبا 3 تا 11درصد از نیوپلاسم های مغزی کودکان را تشکیل می دهند. مطالعه حاضر با هدف تعیین خصوصیات دموگرافیک و بالینی بیماران مبتلا به تومورهای ناحیه پینه آل انجام شد.
روش بررسیاین مطالعه از نوع توصیفی مقطعی بود که در سال 1402 انجام شد.20 بیمار با تومور ناحیه پینه آل بصورت سرشماری شناسایی شدند که در طی 8 سال گذشته به بیمارستانهای شهر اصفهان (الزهرا، کاشانی، امام حسین) مراجعه نموده بودند. داده ها توسط چک لیست جمع آوری و در نرم افزار SPSS ویرایش 22 مورد تحلیل قرار گرفتند.
یافته ها10 نفر (50 درصد) از بیماران مرد و میانه سن بیماران در زمان عمل جراحی 19.25 سال (محدوده 0.16 تا 66 سال) بود. اندازه متوسط تومور 24 میلیمتر و از نظر بافت شناسی، تومور سلول زایا و تومور پارانشیم پینه آل به ترتیب 45 و 25 درصد از نیوپلاسم های ناحیه پینه آل را تشکیل داده بودند.60 درصد از بیماران تحت رادیوتراپی قرار گرفته بودند. سن بالاتر و عدم رادیوتراپی فاکتورهای با تاثیر منفی بر بقا بودند. کمترین نرخ بقا در سال اول بود اما با افزایش تعداد سال های زندگی، نرخ بقا نیز افزایش یافته بود.
نتیجه گیریاز آنجا که بیماران مبتلا به تومورهای ناحیه پینه آل بیشتر در محدوده سنی جوان قرار داشتند و جوانان نیروهای مولد در هر جامعه هستند بنابراین بایستی اقدامات و راهکارهای مناسبی را برای بهبود وضعیت بیماران در بلندمدت اتخاذ نمود تا بتوان تعداد سال های زندگی توام با کیفیت مناسب را برای آنها افزایش داد.
کلید واژگان: تومور مغزی, پینه آل, بیماران}Forensic Medicine, Volume:29 Issue: 3, 2023, PP 151 -156IntroductionThe pineal gland is a small, pinecone-shaped endocrine gland that participates in the biological rhythm regulation of vertebrates. Tumors of the pineal region account for approximately 3–11% of pediatric brain neoplasms. The present study aimed to determine the demographic and clinical characteristics of patients with tumors in the pineal region.
MethodsThis research was a cross-sectional descriptive study that was conducted in 2023. 20 people with pineal tumor were identified who had referred to the hospitals of Isfahan city, Iran (Al-Zahra, Kashani and Imam Hossein) during the last 8 years. Data were collected by checklist and described and analyzed in SPSS version 22 software.
ResultsTen of patients were males and The mean age of the patients at the time of surgery was 19.25 years (range: 16.0 to 66.0 years). Histologically, GCT and PPT comprised 45 % and 25% of pineal region neoplasms. The median tumor size was 24 mm. The rates of radiotherapy administration were 60%. older age, and lack of radiotherapy use were prognostic factors that negatively influence survival. The lowest survival rate was observed in the first year, but as the number of years of life increased, so did the survival rate.
ConclusionGiven that patients with tumors in the pineal region are predominantly in the young age group, and young individuals represent the productive workforce in any society, it is imperative to implement appropriate measures and strategies to enhance these patients' long-term well-being. Implementing these measures and strategies will ultimately improve the overall quality of life for these patients over the years.
Keywords: Region, Tumors, Patients} -
The ectopic endometrial tissue can be found in different places with no symptoms (such as intestinal endometriosis) and common symptoms such as abnormal bleeding, dysmenorrhea, and chronic pelvic pain. Early diagnosis and treatments, especially with surgical procedures, play an important role in patients’ recovery. We describe a 39-year-old woman with intermural and submucosal endometriosis. The compressive effect of the mass in the rectosigmoid colon caused digestive symptoms. After necessary procedures such as colonoscopy, computed tomography (CT) and endoscopic ultrasonography (EUS), we performed surgery, and the distal colon was resected. Ovarian cysts caused by endometrial tissue displacement can have symptoms similar to gastrointestinal stromal tumors (GISTs) if they are large enough to push through the gastrointestinal (GI) system. These symptoms can be diarrhea, abdominal tenderness, and so on. Surgery is the best diagnostic way for endometriomas and one of the diagnostic ways in GISTs. Also, with considering the drug resistance of GISTs to the current chemotherapy, the best treatment is also surgery. Location and tissue involvement of masses of the GI system are important points that should be considered in the differential diagnoses. In this way, early diagnosis and timely treatment, especially surgical, will have the best prognosis for the affected patients.
Keywords: Sigmoidal Endometrioma, Subepithelial Lesion, Gastrointestinal, Stromal, Tumors} -
BackgroundRelatively low incidence has led to an under-rating of fibula tumors. This study aimed to evaluatefibula tumors as a whole and to give detailed information based on histological types according to the anatomiclocation of the tumors in the fibula.MethodsEvaluation was made of all the primary bone tumors of the fibula recorded in our bone tumor registry andinstitute of pathology from 2007 to 2018. Of these, 62 cases were identified. Analysis included assessment of age,gender, tumor localization, the presenting symptoms, the duration of symptoms, and treatment methods.ResultsThere were 48 (77.4%%) benign and 14 (22.6%) malignant tumors. The most commonly found benigntumors were non-ossifying fibroma (12/48; 25%) and aneurysmal bone cyst (12/48; 25%), and the malignant tumorswere chondrosarcoma (3/14; 21.4%) and chondroblastic osteosarcoma (3/14; 21.4%). The most common locationfor both benign and malignant tumors (58.3%, 71.4%) are the proximal fibula, followed by the distal fibula (27.1%,28.6%) and the diaphysis (14.6%, 0%). Six (9.7%) patients prese nted with pathological fibula fractures.ConclusionFibular tumors are rarely encountered in clinical practice but are mostly benign, with malignancydetermined in approximately a quarter of patients. However, as most benign tumors are asymptomatic, and thereforeremain undetected, the actual proportion of malignant tumors wi ll be much lower.Level of evidence: IVKeywords: benign, Distribution, Fibula, Malignant, primary bone tumors, Tumors}
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Background
The venom of different snake species has a distinctive composition. This composition can be also affected by other factors such as age, sex, geographical, and seasonal variations. Generally, snake venom is composed of small molecules such as inorganic cations as well as enzymatic and non-enzymatic peptides, and proteins. Although snake bite poisoning is highly associated with death after systemic absorption of the venom, some studies report on snake venom’s composition, toxicodynamic, and potential therapeutic.
MethodsUsing electronic databases like ISI Web of Knowledge, PubMed, and Scopus, this review aims to point to some components of snake venom and how these components can be used for therapeutic and diagnostic purposes.
ResultsSnake venom was used for the treatment of different pathophysiological conditions in ancient times and is now being used in both modern and folk medicine. These have created the opportunity for scientists to discover new drugs that are more targeted to the site of action and have fewer adverse effects.
ConclusionToday, using special techniques of isolation and formulation, some purified snake venom components are being used for the treatment of acute and chronic conditions, while some others are under further clinical trials. This is due to their potential to produce antitumor, antimicrobial, analgesic, antiplatelet, hypotensive, and other activities.
Keywords: Snake venom, Platelet Aggregation Inhibitors, Analgesic, Tumors} -
Background and Aims
Retinoblastoma tumors are the most common intraocular malignancy in childhood, leading to death after two years. The Human Adenovirus (HAdV) infection could be critical in the retinoblastoma pathogenesis due to the virus and retinoblastoma 1 interactions. The objective of the current study was to investigate the possible presence of the HAdV genome in the retinoblastoma patientchr('39')s tumors.
Materials and MethodsIn this study, we evaluated the HAdV infection in 96 pathological confirmed retinoblastoma samples. The DNA was extracted from formalin-fixed paraffin-embedded blocks, and the virus infection was assessed using polymerase chain reaction. SPSS version 22 was used for statistical analysis.
ResultsThe mean age ± SD of the retinoblastoma patients was 28.89 ± 17 months. In addition, the demographic evaluation indicated that 43 (46.7%) of patients were female. The retinoblastoma laterality assessment indicates 87 (90.4%) unilateral and 9 (9.4%) bilateral tumors. Growth pattern analysis indicates endophytic 58 (77.3%), exophytic 8 (10.7%), and 9 (12%) of tumors with mix endophytic and exophytic patterns. The polymerase chain reaction results could not found any evidence of HAdV infection in all 96 formalin-fixed paraffin-embedded samples.
ConclusionsThe study results suggest that there is not any association between HAdV infection and retinoblastoma tumors in studied samples. The HAdV infection may not a concern in retinoblastoma pathogenesis. Further investigations are recommended in this field of study.
Keywords: Human adenovirus, PCR, Retinoblastoma, Tumors} -
Background
Bilateral synchronous testis germ cell tumors with different histopathology are not common.
Case PresentationHere, a case of 27-year-old male who is reported presented with bilateral testicular swellings. There was a high α-fetoprotein level with bilateral lesions on scrotal USG. Bilateral orchiectomy was performed. According to pathology report, there was a right testicular seminoma and left testicular mixed germ cell tumor composed of seminoma, yolk sac tumor and embryonal carcinoma.
ConclusionHe received one cycle of chemotherapy with BEP regimens
Keywords: Testis, Tumors, Histology} -
Background
The clinical and imaging presentations of primary tumors and tumor-like lesions in the clavicle are not clear.
ObjectivesTo investigate the clinical and imaging presentations of primary tumors and tumor-like lesions in the clavicle for better diagnosis.
Patients and MethodsPatients with clavicular diseases between 1963 and 2018 confirmed by pathology who had plain radiography, computed tomography (CT) scan and magnetic resonance imaging were enrolled. The age, sex, imaging data, radiological signs and location of the tumor at the clavicle of patients were analyzed and compared.
ResultsEighty-one patients with clavicular diseases were identified including 49 males and 32 females with an age range of 2 - 76 years (mean, 42.6). There were malignant tumors in 50 cases (61.7%), intermediate in 12 (14.8%), and benign in 19 cases (23.5%). Malignant tumors included metastatic tumors in 31 cases (38.3%), plasma-cell myeloma in ten (12.3%), and osteosarcoma in four (4.9%). The intermediate bone tumors were mainly eosinophilic granuloma in six cases (7.4%), and aneurysmal bone cyst in three (3.7%). Benign tumors were mainly osteochondroma (6.2%), bone cyst (3.7%), and chondroma (3.7%). Malignant tumors had bone destruction, periosteal reaction, ill-defined margins and soft tissue masses. Benign tumors and tumor-like lesions had well-defined margins.
ConclusionsMany tumors may occur at the clavicle with more malignant than benign tumors with no specific imaging features in most lesions. A lesion near the sternal end with atypical benign imaging features should be considered as malignant.
Keywords: Malignant, Tumors, Clavicle, Imaging, Benign, Tumor-Like Lesion} -
Background
Osteoid osteoma (OO) is a benign tumor that rarely occurs in carpal bones. Occurrence of OO in trapezoid is extremelyrare. We present a patient with OO of the trapezoid as 7th reported case around the world.
Case PresentationA 25-year-old man was referred to our clinic with a 12-month history of pain of his left wrist. He mentioned that hehad wrist pain during manual activity and the pain was increasing over time. He did not have history of trauma. He was treated with nonsteroidal anti-inflammatory drugs (NSAIDs) before being referred to our clinic; however, it did not work. Examination showed tenderness over the dorsoradial side of the left wrist. Conventional radiographs of the wrist were normal. Computed tomography (CT) demonstrated a halo radiolucent osteoid tissue surrounded by a sclerotic tissue in left trapezoid. Magnetic resonance imaging (MRI) showed a focal hypointense lesion (nidus) in the trapezoid with 10 mm diameter. A focal increased uptake of 99mTc in his trapezoid was shown by bone scintigraphy. According to the clinical and imaging findings, we considered excisional biopsy with the diagnosis ofOO of trapezoid bone. Surgery was performed through a dorsal incision. We performed en bloc excision. Histopathological findings confirmed the diagnosis of OO. The patient got pain-free on postoperative day 3.
ConclusionsCarpal bones tumor such as OO should be considered in differential diagnosis of patients with chronic wrist pain.
Keywords: Osteoid Osteoma, Wrist, Tumors} -
BACKGROUND AND AIM
Benign fibrous histiocytoma (BFH) is a rare lesion in the head and neck with a slow, single, and painless growth that consists of fibroblasts and histiocytes. In this study, a BFH case was reported and examined from clinical, microscopic, and immunohistochemical aspects.
CASE REPORTA 36-year-old man with a red nodule on the dorsal surface of his tongue was referred to the oral medicine department. The appearance of this nodule was similar to the adjacent tissue in its surface. According to the same microscopic view of this lesion with other soft tissue tumors, immunohistochemistry test confirmed the diagnosis. It was treated with en-bloc surgical resection. In four follow-ups up to one year, there was no recurrence. Considering the results of these cases and comparing them with other cases, although there is a slim chance of recurrence in one year, follow up is recommended.
CONCLUSIONClinical view of FH is not characteristic and tumors with microscopic spindle-shaped appearance are challenging in diagnosis. IHC is obligatory to reach a prompt diagnosis and due to recurrence, follow-up is recommended.
Keywords: Histiocytoma, Benign Fibrous, Tumors, Tongue Disease, Oral Cavity} -
مقدمهتومورهای تخمدانی حد واسط (Borderline)، از دسته ی پاتولوژی های اپی تلیالی تخمدان هستند. با توجه به شیوع این تومورها در سنین باروری، اهمیت پیش آگهی و درمان استاندارد این بیماران جایگاه ویژه ای در مطالعات انکولوژی یافته است. از این رو، مطالعه ی حاضر با هدف ارایه ی گزارش دو مورد مبتلا به توده ی تخمدان با پاتولوژی حد واسط و بررسی موارد تعیین کننده ی پیش آگهی بر اساس مطالعات مشابه انجام شد.گزارش مورددر زمستان سال 1397، دو بیمار جوان با تاریخچه ی طبی مشابه از کیست تخمدان تشخیص داده شدند. این دو بیمار در سال 1394 با پاتولوژی مشابه تومور حد واسط تخمدانی مرحله ی یک، به اورژانس یک بیمارستان دانشگاهی مراجعه نموده بودند. بیمار نخست، خانم 29 ساله ای است که به دنبال جراحی با هدف حفظ باروری، دچار عود و متاستاز بدون پاسخ مناسب به درمان شده بود و با وجود تمامی تلاش کادر درمان، جان خود را به دلیل وسعت بیماری از دست داده بود. بیمار دیگر، خانم 26 ساله ای است که در سن بارداری 36 هفته و با تشخیص پره اکلامپسی بستری و نوزاد سالمی با وزن 2800 گرم زایمان نموده بود.نتیجه گیریاگر چه انتظار می رود تومور حد واسط تخمدان، پیش آگهی متفاوتی از بدخیمی های تخمدانی داشته باشد، اما با توجه به موارد گزارش شده در این مطالعه، به نظر می رسد بررسی عوامل موثر در پیش آگهی هر بیمار به صورت مجزا ضرورت داشته باشد.کلید واژگان: رحم, تومورها, حفظ باروری, بررسی ژنتیک, نشانگر تومور, پیش آگهی}Background
Borderline ovarian tumors make a small contribution to the ovarian pathologies; however, with regard to the prevalence of this malignancy at reproductive age, prognosis and standard treatment of these patients are of great significance in oncology trials. The present study aimed to introduce two patients with borderline ovarian tumors to examine the prognosis determinants based on similar studies.Case ReportIn the winter of 2018, two patients with similar medical history of ovarian cysts diagnosed in 2016 with stage I epithelial ovarian tumor (borderline) pathology referred to an emergency department in a university hospital. The first patient was a 29-year-old woman. Following the surgery to preserve her fertility, the mentioned patient experienced relapse and metastases without any proper responses to treatment. Despite all the efforts of the medical team, the patient died due to the severity of her disease. The other patient was a 26-year-old woman, who was admitted at 36th week of pregnancy with the diagnosis of preeclampsia, and delivered a 2800-gram healthy boy.ConclusionAlthough it seems that borderline tumor is distinct from other ovarian malignancies in term of prognosis, based on the present case report, the prognosis must be investigated in each patient in individualize manner.Keywords: Ovary, Tumors, Fertility preservation, Genetic testing, Markers, Tumor, Prognosis} -
سابقه و هدفلوسمی میلوئیدی حاد یک سرطان ناهمگن است که از طریق مکانیسم های مختلف پاتولوژیک ایجاد می شود. سلول های سرطانی، سیستم کموکاین را دستخوش تغییر می نمایند. گیرنده CCR5 ، اثر غیر مستقیمی بر پیشرفت سرطان توسط کنترل پاسخ ایمنی علیه تومور دارد. این گیرنده می تواند رشد تومور را تسریع و در متاستاز آن نقش به سزایی ایفا کند. در تحقیق حاضر برآن شدیم تا با بررسی گیرنده CCR5 در بیماران AML بعد از شیمی درمانی مرحله اول، تا حدودی به بررسی نقش احتمالی این رسپتور بپردازیم.مواد و روش هااین مطالعه مورد شاهدی در سال 1397-1396 در دانشگاه علوم پزشکی کرمان انجام شد. 25 بیمار مبتلا به AML با تمایز منوسیتی، پس از شیمی درمانی مرحله اول (هفته چهارم پس از شیمی درمانی) و بعد از بررسی لام خون محیطی و تائید عدم وجود بلاست، توسط فلوسیتومتری برای بیان گیرنده کموکاینی CCR5 بر جمعیت لکوسیت های خون محیطی با گروه کنترل سالم مقایسه شدند. یافته ها توسط آزمون t دو نمونه ای مستقل و 22 SPSS تجزیه و تحلیل شدند.یافته هامطالعه حاضر نشان داد که میانگین بیان گیرنده CCR-5 در گروه بیماران بعد از شیمی درمانی(26/0 ± 04/1) مشابه با گروه کنترل سالم(16/0 ± 04/1) بوده است و تفاوت معنا داری بین این دو گروه وجود نداشت.نتیجه گیریشیمی درمانی سبب شده است که بیان گیرنده CCR5 در حالت پایه خود در مقایسه با گروه کنترل سالم قرار گیرد. می توان سایر محورهای کموکاین و گیرنده های آن ها را مورد بررسی قرار داد تا پی ببریم کدام یک نقش به سزایی در عود بیماران خواهد داشت.کلید واژگان: لوسمی میلوئید حاد, گیرنده کموکاین, گیرنده CCR5, شیمی درمانی}Background and ObjectivesAcute myeloid leukemia (AML) is a heterogeneous cancer that is caused by various pathologic mechanisms. Cancer cells change the chemokine system. CCR5 receptor has an indirect effect on cancer progression by controlling immune response against the tumor. This receptor can accelerate tumor growth and play a significant role in tumor metastasis, and it has been shown that CCR5 antagonists inhibit tumor growth. In this study, we decided to investigate the CCR5 receptor in AML patients after the first stage chemotherapy.Materials and MethodsThis case-control study was conducted in Kerman University of Medical Sciences during 2017-2018. Twenty five AML patients with monocytic differentiation post the first stage of chemotherapy (the fourth week after chemotherapy), after being examined for the peripheral blood smear and confirmed for the absence of blast cells, were evaluated by flow cytometry for the expression of the CCR5 receptor on the peripheral blood leukocytes population and were compared with healthy controls. The data were analyzed by independent T-Test and SPSS (version 22).ResultsThe results of this study showed that the mean expression of CCR-5 in the patients group post-chemotherapy (1.04 ± 0.26) was similar with the healthy control group (1.04 ± 0.16). Moreover, there was no meaningful difference between the two groups.ConclusionsChemotherapy has caused the CCR5 receptor expression to be in its base state compared to the healthy control group. Other chemokine syndromes and their receptors could be examined to find out which role would play a significant role in the recurrence of patients.Keywords: Acute Myeloid Leukemia, Chemotherapy, Monocytes, Tumors}
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BACKGROUNDEpithelial cell adhesion molecule (EpCAM) is an adhesion molecule which is expressed on the epithelial cells and primarily identified as a tumor marker for carcinoma. In this study, the expression of EpCAM in precancerous and cancerous gastric lesions was investigated and then, the association of EpCAM expression with the overall survival of patient suffering from gastric carcinoma was evaluated.METHODS12 gastric carcinoma, 3 dysplasia, and 8 intestinal metaplasia (IM) subjects were taken from the department of pathology of Tohid Hospital, Sanandaj, Iran. The diagnosis was made by the expert pathologist. Then, the subjects were stained for EpCAM by immunohistochemistry (IHC) and analyzed by the pathologist.RESULTSThe data showed that EpCAM was expressed in all of the precancerous and cancerous samples. However, 76.4% of carcinoma cells were positive for EpCAM while it was 62.5% and 51.3% for dysplasia and IM, respectively. Importantly, it was observed that the expression of EpCAM on gastric cancer was negatively correlated with the overall survival of the patients.CONCLUSIONIn conclusion, it was demonstrated in this study that EpCAM is expressed in gastric carcinoma and its expression is negatively correlated with the overall survival of the patients with gastric cancer.Keywords: Epithelial Cell Adhesion Molecule, Gastric Cancer, Tumors}
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Background
Osteoid osteoma (OO) is a benign osteoblastic neoplasm, mostly occurring in long bones of lower extremity. Its manifestation in unusual locations can be a diagnostic challenge and distressing for patients. OO in carpal bones is uncommon; its occurrence in triquetrum is even more so.
Case PresentationThis study reports on a nineteen-year-old female with history of wrist pain for 4 years. She had sustained trauma to the same wrist before commencing of pain. Patient's pain was unresponsive to conservative treatments. Her routine x-rays were mostly interpreted as normal and obtaining further imaging helped us in diagnosis of OO of triquetrum. Surgical resection of the nidus was performed.
ConclusionsManifestation of OO in small carpal bones may not be typical; identifying the lesion or nidus could be challenging. Whatever unusual the location or presentation of such lesions may be, obtaining advanced imaging can be of significant help; therefore, we suggest clinicians to have low threshold in ordering advanced imaging specifically in patients suffering from chronic pain. Also, persistent history of nocturnal pain is a sign which is worth attention
Keywords: Osteoid Osteoma, Tumors, Diagnosis, Carpal Bones, Triquetrum Bone} -
Hydatid cyst is a parasitic disease that is endemic in Mediterranean areas, South America, North Africa, Australia, and Iran. Although the liver and lung are the most common involved organs, but the other organs in human body also can be involved by hydatid cyst. Chest wall involvement by hydatid cyst is a rare condition, which may be misdiagnosed as chest wall tumor in the endemic areas. Herein, we presented a case of primary chest wall hydatid cyst mimicking chest wall tumor.Keywords: Chest Wall, Hydatid Cyst, Resection, Tumors}
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مقدمهمطالعات متعدد ثابت نمودهاند که سلول های سرطانی انسان می توانند در نتیجه آلودگی به ویروس هرپس سیمپلکس به وجود آیند. با توجه به مشاهده حضور DNA این ویروس در بافت پارافینه سرطان پستان در برخی از نمونه های توموری این احتمال وجود دارد که ویروس هرپس سیمپلکس می تواند یک فاکتور خطر برای شکل گیری کارسینومای پستان باشد.
هدف از اجرای این تحقیق بررسی میزان فراوانی RNA وDNA ویروس هرپس سیمپلکس انسانی در نمونه های تومورتازه و پارافینه شده پستان می باشد.روش بررسیدر این بررسی 70 نمونه تازه و پارافینه شده تومور پستان از بیماران مبتلا به سرطان پستان که در بیمارستان های گلسار، آریا و رسول اکرم(ص) رشت در سال 1395 جراحی شده، بودند جمع آوری گردید. پس از انتقال سریع نمونه ها به آزمایشگاه، استخراج RNA و DNA با استفاده از کیت (Genall Korea) انجام گردید. سپس با استفاده از کیت یک مرحله ای (GenallKorea)، RNA استخراجی به cDNA تبدیل گردید. در ادامه به منظور تکثیر ژن UL30 ویروس هرپس سیمپلکس از پرایمر اختصاصی، استفاده شد.
یافته ها: در مجموع از 70 نمونه سرطان پستان هیچ نمونه مثبتی در بررسی بافت تازه و پارافینه مشاهده نشد که این مسئله نشان دهنده عدم حضور ژنوم ویروس هرپس سیمپلکس در تومور پستان در این تحقیق می باشد.
نتیجه گیری: در حدود یک دهه است که نقش هرپس ویروس ها در شکلگیری سرطان های سرویکس، هودچکین، لنفوم بورکیت و سرطان عروق خونی ثابت شده است. با این حال شواهدی نیز وجود دارد که موفق به شناسایی ژنوم ویروس HSV در تومورها نشده اند از اینرو مطالعات بیشتر برای درک ارتباط این ویروس ها با شکل گیری تومورهای سینه نیاز می باشد.کلید واژگان: سرطان پستان, تومور, ويروس هرپس سيمپلکس, PCR}IntroductionSeveral studies have proven that human cancer cells can develop as a result of infection with the herpes simplex virus. Regarding this observation, the presence of this virus DNA in the paraffin tissue of breast cancer in some tumor samples can be a risk factor for the formation of breast carcinoma. The aim of this study was to investigate the frequency rate of RNA and DNA of human herpes simplex virus in fresh and paraffined breast tumor samples.MethodsIn this study, 70 fresh and paraffined breast tumor samples were collected from patients with breast cancer that were surgically treated in Golsar, Aria, and Rasoul-e-Akram hospitals on Rasht, Iran, in 2016. After rapid transfer of samples to the laboratory, RNA and DNA extraction was performed using one-stage kit (Genall, Korea), and the extracted RNA was converted to cDNA. Next, the UL30 gene of herpes simplex virus from exclusive primer was used for proliferation.ResultsOut of 70 samples of breast cancer, none was positive in the fresh and paraffined tissues. This issue indicates the absence of the genome of herpes simplex virus in the breast tumor in this study.ConclusionsThe role of herpes viruses has been proven in the formation of cervical cancers, Hodgkins, Burkitt Burkitts lymphoma, and blood vessels cancer in the past decade. However, there is also evidence that HSV genome was not identified in tumors. Therefore, further studies are needed to understand the association of these viruses with the formation of breast tumors.Keywords: Breast Cancer, Tumors, Herpes Simplex Virus} -
مقدمهاین مطالعه، با هدف تعیین ارزش تشخیصی حین عمل جراحی روش Frozen section در مقایسه با نتایج پاتولوژی نهایی نمونه های تثبیت شده در فرمالین در تعیین ماهیت توده های سر و گردن به انجام رسید.روش هادر یک مطالعه ی توصیفی- تحلیلی، کل 88 نمونه ی مربوط به توده های سر و گردن که از سال های 94-1389 در بیمارستان الزهرای (س) اصفهان موجود بود، مورد مطالعه قرار گرفت و نتایج روش Frozen section و پاتولوژی توده ی آن ها از پرونده ی بیماران استخراج گردید. سپس، حساسیت، ویژگی، مثبت و منفی کاذب و ارزش اخباری این روش در مقایسه با پاتولوژی محاسبه گردید.یافته هاروش Frozen section در مقایسه با نتایج پاتولوژی نهایی نمونه های تثبیت شده در فرمالین، دارای حساسیت 8/89 و ویژگی 4/94 درصد بود. درصد مثبت و منفی کاذب این روش، به ترتیب 6/5 و 2/10 درصد به دست آمد. ارزش اخباری مثبت و منفی آن نیز به ترتیب 7/95 و 2/87 درصد بود. میزان صحت این روش 8/91 درصد به دست آمد.نتیجه گیریروش Frozen section حین عمل جراحی جهت تعیین ماهیت توده های سر و گردن، روشی به نسبت دقیق و با ارزش است، اما لازمه ی آن، تجربه ی کافی آسیب شناسان شاغل در واحدهای پاتولوژی است که در صورت انجام صحیح آن و همچنین، دقت در نمونه گیری توسط جراح و همکاری این دو، می تواند افزایش میزان صحت Frozen section و در نهایت، کاهش اعمال جراحی مجدد، کاهش عود و پیش آگهی مطلوب تر بیماری را به دنبال داشته باشد.کلید واژگان: Frozen section, پاتولوژی نهایی, حساسیت, ویژگی, سر, گردن, توده}BackgroundThis study aimed to determine the diagnostic values of frozen section compared with permanent pathology results for detection of characteristic of head and neck tumors.MethodsIn a cross-sectional study, 88 patients suffered from head and neck tumors and operated during 2010-2015 in Alzahra hospital, Isfahan, Iran, were enrolled. The results of frozen section and permanent pathology were extracted from hospital records and sensitivity, specificity, false negative, false positive, and negative and positive predictive values were calculated for frozen section.
Findings: Sensitivity, specificity, false negative, false positive, positive predictive value, and negative predictive value were as 89.8%, 94.4%, 5.6%, 10.2%, 95.7%, and 87.2%, respectively; and the accuracy of frozen section was 91.8%.ConclusionFrozen section test during surgeries is a good and valuable method for detection of characteristic of head and neck tumors. But, enough pathologist experience and precision of sampling by surgeon can lead to increase the accuracy rate of frozen section which finally leads to decrease of reoperation and relapse of disease, and better prognosis.Keywords: Frozen sections, Permanent pathology, Sensitivity, Specificity, Head, Neck, Tumors} -
Breast cancer affects Iranian women at least one decade younger than their counterparts in other countries and the incidence of breast fibroadenoma is growing in the last two decades in Tehran. This study aimed to compare the AhR levels in premenopausal breast cancer and breast fibroadnemo with appropriate normal groups. Possible associations of AhR with lifestyle and reproductive risk factors and other fundamental genes of breast cancer and reproductive disorders were the other major goals of present study. To conduct the comparisons all possible reproductive, environmental and lifestyle risk factors of mentioned diseases were recorded in 100 breast cancer, 100 breast fibroadenoma and compared with 400 women in normal group from 2009 to 2011. AhR overexpression in epithelial cells of premenopausal patients emphasized the susceptibility of these cells to environmental induced reproductive disorders. The AhR overexpression was contributed to ER-/PgR- immunophenotype in malignant tissues. Weight gain (after 18 and after pregnancy), long term (>5yrs) OCP consumption, smoking, severe stress ,history of ovarian cysts, hormonal deregulations, living near PAHs producing sources, were correlated with increased risk of breast cancer and reproductive disorders and were correlated with elevated tissue levels of AhR. It seems that increased risk of breast cancer and other reproductive tumours in Tehran may be the result of exposure to environmental endocrine disruptors. Long term exposure to environmental estrogens can increase the tissue levels of AhR and deregulate the expression pattern of sex steroid receptors and other genes in target tissues.Keywords: Endocrine Disrupting chemicals, Steroids, Breast cancer, Tumors}
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IntroductionPituitary adenomas have been the most common sellaturcica tumors. There have been many unusual types of pituitary tumors that might neglect by radiologists and clinicians. One of these tumors would be the malignant glioma.Case PresentationA 62-year-old male has complained from sudden frontal headache, nausea, vomiting, decreased vision, blurred vision and double vision. In skull radiographic, there was an expansion of sellaturcica and a lesion with clear border on T1; heterogeneous; iso - to hypotense; size about 3/5 × 2/5 cm with no surrounding edema that it has homogeneously attracted contrast Lesion, that shown a signal hypointensity on T2 with heterogeneous enhancement. In the coronal sections, the tumor expanded to the suprasellar region and optic chiasmatic that has compressed especially on the left side. Partial tumor resection has conducted. The surgery has done by a transsphenoidal approach. The pathologist has diagnosed a glioblastoma. This diagnosis has confirmed using immunohistochemistry technique.ConclusionsThere have been many unusual types of pituitary tumors that might neglect by radiologists and clinicians. One of these tumors would be the malignant glioma.Keywords: Tumors, Glioblastoma, Pituitary Adenoma}
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BackgroundIrreversible electroporation (IRE) is a relatively new approach to the management of multiple types of locally advanced soft tissue tumors. Unique peri-procedural anesthetic management is needed in the safe and effective delivery of this therapy..ObjectivesThis study analyzed IRE therapy in relation to anesthetic management for our initial cohort and then established and validated a set of best practical guidelines for general anesthesia in patients undergoing IRE for abdominal tumors..Patients andMethodsAn IRB-approved prospective data collection outcome protocol was utilized. This study was broken up into two cohorts as follows: the initial 38 patients (pts) undergoing IRE in which anesthetic management was not defined or optimized and then a 40-pt validation cohort to establish the most efficacious anesthetic protocols..ResultsDuring IRE delivery, a deeper neuromuscular blockade is required to ensure that all retroperitoneal muscle excitation was minimized. In the initial 38-pt cohort, attempts to treat hypertension (median SBP 190, range 185–215 and median diastolic 98, range 91–115) were made with various types of anti-hypertensives with minimal-to-insufficient effects. The established inhalation was sevoflurane with an approximate median dose of 8.0 volume percentage. Analgesic management of continuous remifentanil was utilized with epidural management, which optimized HTN and tolerance to IRE therapy..ConclusionsAnesthetic management for IRE of soft tissue deviates from standard anesthetic medical therapy in regards to depth of neuromuscular blockade and analgesic management during IRE energy delivery. However, minor modifications in anesthesia management allow for a safe and efficient patient procedure..Keywords: Anesthetic, Electroporation, Tumors}
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