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CD56-positive Angioimmunoblastic T-cell Lymphoma Complicated by Chylothorax.
Intern Med
March 2022
Department of Hematology, Japanese Red Cross Wakayama Medical Center, Japan.
A 77-year-old woman presented with systemic lymphadenopathy and bilateral pleural effusion. Angioimmunoblastic T-cell lymphoma (AITL) was diagnosed based on the results of a lymph node biopsy. AITL cells expressed the aberrant antigen of CD56.
View Article and Find Full Text PDF[Chylothorax due to angioimmunoblastic T-cell lymphoma: a case report].
Zhonghua Xue Ye Xue Za Zhi
October 2020
Department of Hematology, Beijing Institute of Respiratory Medicine and Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, China.
A Rare Case of Angioimmunoblastic T-Cell Lymphoma with Epstein-Barr Virus-Negative Reed-Sternberg-Like B-Cells, Chylous Ascites, and Chylothorax.
Case Rep Hematol
April 2017
Department of Pathology, VieCuri Medical Centre, 5912 BL Venlo, Netherlands.
Angioimmunoblastic T-cell lymphoma is a rare non-Hodgkin lymphoma with dismal prognosis. The median age of presentation ranges from 62 to 69 years with generalized lymphadenopathy, B symptoms, and hepatosplenomegaly as the most prevalent symptoms. The combination of B-cell and T-cell proliferations is common in AITL and the B-cell component may resemble Reed-Sternberg-like B-cells.
View Article and Find Full Text PDFChylothorax in a case of Non-Hodgkin's lymphoma.
J Coll Physicians Surg Pak
February 2003
Department of Pulmonology, Military Hospital, Rawalpindi.
A case of asymptomatic 60 years old male diagnosed as Non-Hodgkin's lymphoma (angioimmunoblastic T-cell type) invading thoracic duct leading to chylothorax is presented. Generally, patients with this moderately aggressive lymphoma are adults who exhibit generalized lymphadenopathy, B-symptoms, polyclonal hypergammaglobulinemia, skin rash and various autoimmune phenomena.
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