جستجوی مقالات مرتبط با کلیدواژه "burkitt lymphoma" در نشریات گروه "پزشکی"

As a new point, some very rare features can be revealed as initial diagnosis of acute lymphoblastic leukemia (ALL) without any evidence of lymphoma-like behavior which after initial recovery, presents with new evidence of lymphoma. Herein, a case of the immunophenotypes of blast cells in B-cell precursor acute lymphoblastic leukemia originated from MYC gene-related that was evidenced later by burkitt lymphoma feature.

Our case was initially diagnosed as a typical B-cell ALL cells with L1 morphology in peripheral blood smear and bone marrow aspiration that was not recovered and referred again that was finally featured as burkitt’s lymphoma with L3 morphological feature.

Thus, in the primary diagnosis of B-cell ALL and especially in cases with treatment failure, the final feature of burkitt’s lymphoma should be potentially in mind.

Primary Burkitt lymphomas of the chest wall are relatively rare in occurrence. The authors describe a first case report in Malagasy child. It presents as an isolated soft-tissue mass on the chest wall with a sudden installation of paraplegia in an 8-year-old girl. Our patient was treated with aggressive chemotherapy regimen with complete remission on 2 years of follow-up.

Burkitt lymphoma is an aggressive subtype of Hodgkin lymphoma with a doubling time of 25 hours. It is characterized by a MYC gene coding alteration which results from a translocation of chromosome 8 on the MYC gene locus and immunoglobulin heavy-chain locus (IGH) on chromosome 14. Even though HIV infection is associated to an increased risk of Burkitt lymphoma, these type of malignancies are EBV-negative cases. Sporadic type Burkitt lymphoma is a rare clinical entity. A 48-year-old female without any past medical history presented with a chief complaint of mild abdominal pain of 6 months duration located at the epigastrium which was not related to food ingestion. Nausea or vomiting were neither reported. She noted an acute increased abdominal pain over the last 4 hours before presentation, with irradiation to the right lower quadrant. She denied any Fever, night sweats and weight loss. She also reported hypermenorrhea in the last 6 months. During the physical examination, a palpable mass with 10 cm in diameter was found on right lower quadrant. Sporadic Burkitt lymphoma is one of the rarest hematologic malignancies. The increased tumor size may be more than enough to show clinical or biochemical abnormalities such as serum lactate dehydrogenase (LDH) increased and tumor lysis.

We present a 13.5 year old boy with chronic intussusception that was misdiagnosed as Crohn disease and received treatment for the wrong diagnosis. Because his condition didn’t improve, more work-ups were performed and the radiologic work-ups revealed the diagnosis of a missed intussusception with fistula.We suggest that prolonged intussusception should be considered in the list of differential diagnosis for the refractory abdominal pain and distention, bloody diarrhea, and radiologist consultancy should be requested, as Crohn disease, infectious gastroenteritis, abdominal malignancies and prolonged intussusception should be carefully investigated and considered in such situations.

Lymphoma is the most common malignancy originating from hematopoietic systems. Diverse biological and clinical manifestations of non-Hodgkin lymphoma have been recognized. As an unusual type of non-Hodgkin lymphoma is Burkitt lymphoma. The variability of the initial presentation is not unusual. We present a 15-year-old boy with
generalized abdominal pain, fever. He had massive orange pleural effusion and ascites. There were peritoneal seeding and omentum thickening in abdominal computed tomography scan. Pathological investigations of the peritoneal biopsy revealed B-cell lymphoma (starry sky in pathology). The clinical presentation of sporadic Burkitt lymphoma could mimic some other diseases. Therefore, the clinicians should consider Burkitt lymphoma between the multiple differential diagnoses. In the case of peritoneal involvement, its differential diagnosis could be usually, peritoneal carcinomatosis, malignant peritoneal mesothelioma, and tuberculous peritonitis.

Primary gastric lymphoma (PGL) is a rare tumor, whose differential diagnosis may become complicated without precise immunohistochemistry (IHC) and genetic analysis.
A 33-year-old woman presented with gastric cancer and had undergone gastrectomy without precise IHC and staging in another center. Inappropriate IHC after surgery showed diffuse large B-cell lymphoma. After her admission to our center, due to gastrointestinal (GI) symptoms further evaluations were performed, leading to application of chemotherapy and radiotherapy regimens. In the next admissions, involvement of tibia, jaw, and gingiva took place and Burkitt lymphoma was diagnosed with precise IHC panel, which made alteration in the treatment. In the last admission, she expired due to renal failure and tumor lysis syndrome.
There was some mismanagement in this case, especially incomplete and inappropriate IHC panel, which led to wrong diagnosis.

Burkitt lymphoma (BL) is rare, but an aggressive malignancy. Central nervous system Burkitt lymphoma (CNSBL) is very rare. CNS Burkitt’s lymphoma is treated with high-dose chemotherapy and radiation. Radiotherapy in children younger than three years old may cause major CNS damage.
Case report: A three-year-old boy presented with painful proptosis of the left eye. He underwent adenoidectomy 2 months before admitted to our center. Sleep difficulty was not resolved after surgery. Microscopic study of paranasal sinus biopsy and IHC confirmed the diagnosis of Burkitt Lymphoma.
Inany patients presenting with painful proptosis, BL should be considered. Adenoid hyperplasia should not be considered as a sole cause of sleep difficulty.

An important complication of chemotherapy is thromboembolic events that can occur during treatment course. In this way, Warfarin can be used as an efficient prophylactic agent to prevent these complications. Although bleeding is a common adverse effect of Warfarin, eosinophilia is a rare side effect of this drug. We have reported a 5-year-old boy with Burkitt lymphoma who underwent chemotherapy. In the course of chemotherapy, because of thrombosis of the left jugular vein, we initiated Warfarin as a prophylactic drug for TEE secondary to chemotherapy. Following Warfarin initiation, eosinophilia appeared and subsequent to cessation of drug, eosinophilia disappeared.This case is presented to point out physicians to consider eosinophilia as a rare adverse-effect of Warfarin and monitor blood cell differentiation regularly during the course of treatment with this drug.

Burkitt lymphoma of stomach is among the most rapidly growing gastric cancersassociated with several gasterointestinal symptoms including hematemesis, anorexia, vomiting and etc. Gastric perforation in patients with Burkitt lymphoma of stomach is a very rare condition especially after chemotherapy. We herein present a 21-year old man who was kwon case of gastric Burkitt lymphoma who had undergone chemotherapy and presented with acute onset gastric pain and tenderness. He was diagnosed to suffer from perforated gastric lymphoma for which laparotomy and total gastrectomy was performed. Treatment was continued by chemotherapy. Closed observation is thus recommended for those patients with gastric Burkitt lymphoma undergoing chemotherapy.

Primary breast lymphoma (PBL) of the breast is a rare type of localized non-Hodgkin lymphoma, which is usually of the B-cell. The majority of breast lymphoma present as a unilateral painless breast masses in an older woman, average age at diagnosis 55-60. A less common but distinctive presentation is a young woman of childbearing age who presents during or immediately after pregnancy. We present a 23-year-old postpartum woman with bilateral breast swelling. After surgical drainage and debridement and pathologic examination, the diagnosis of breast Burkitt lymphoma (BL) was confirmed. Chemotherapy was immediately started for her and the patient showed a good response with complete remission.