A Case of T-Cell Lymphoma Accompanying Marked Eosinophilia, Chronic Eosinophilic Pneumonia and Eosinophilic Pleural Effusion. A Case Report

1991 ◽  
Vol 77 (6) ◽  
pp. 527-530 ◽  
Author(s):  
Akira Kawasaki ◽  
Yutaka Mizushima ◽  
Shoko Matsui ◽  
Kiyoshi Hoshino ◽  
Saburo Yano ◽  
...  

A 57-year-old woman was admitted to our hospital for lumbago, weight loss and weakness of her right lower extremity. Leukocytosis was evident with marked eosinophilia (65.5 % = 46,000/mm3), and the chest roentgenogram showed diffuse reticular shadows throughout both lung fields and a left pleural effusion. The pleural effusion contained 22.4 % eosinophils with no immature cells. Biopsy of a thumb-sized mass on the chest wall revealed a T-cell lymphoma of pleomorphic type. The diffuse pulmonary shadow was diagnosed as chronic eosinophilic pneumonia by autopsy. This was a relatively rare case of T-cell lymphoma, in which an eosinophilic pneumonia and eosinophilic pleural effusion were observed.

2007 ◽  
Vol 106 (2) ◽  
pp. 156-160 ◽  
Author(s):  
Chia-Jung Chang ◽  
Jen-Hsun Cheng ◽  
Ming-Shian Lin ◽  
Yuan-Chang Dai ◽  
Tzuen-Ren Hsiue

Author(s):  
Boaz Hirshberg ◽  
Mordechai R. Kramer ◽  
Michal Lotem ◽  
Vivian Barak ◽  
Larisa Shustin ◽  
...  

1997 ◽  
Vol 36 (6) ◽  
pp. 654-655
Author(s):  
Naoko YAMAUCHI ◽  
Teruaki OKA ◽  
Tsuyoshi ISHIDA ◽  
Hajime HORIUCHI ◽  
Atsuhiko SAKAMOTO

Author(s):  
sasikanth Nallagatla ◽  
Viswanath P. Vasudevan ◽  
Farhad Arjomand ◽  
Rana Ali

2007 ◽  
Vol 46 (11) ◽  
pp. 739-742 ◽  
Author(s):  
Keisuke Hosoki ◽  
Shinji Okada ◽  
Ryo Ichinohasama ◽  
Masaaki Yamaguchi ◽  
Bine Uchiyama ◽  
...  

2000 ◽  
Vol 44 (6) ◽  
pp. 1040-1044 ◽  
Author(s):  
Toshiaki Moriki ◽  
Masayo Wada ◽  
Tamotsu Takahashi ◽  
Shousuke Ueda ◽  
Eriko Miyazaki

2020 ◽  
Vol 3 (1) ◽  

Rationale and Objectives: Subcutaneous panniculitic T-cell lymphoma (SPTCL) is a rare neoplasm accounting for less than 1% of pediatric Non-Hodgkin Lymphomas. It is most common in young adults with predominance of female cases at 0.5. Symptoms include multiple nodules involving the subcutaneous tissues of the extremities and trunk, neck and face. B symptoms such as fever, chills, night sweats and weight loss, have been reported. Rare extra-cutaneous manifestations include edema, involvement of the bone marrow, lymph nodes, liver, spleen, lungs and viscera. Laboratory abnormalities such as cytopenias and elevated lactate dehydrogenase have been recorded. Hemophagocytic syndrome (HPS) occurs in 33% of cases, which were correlated with fatal outcome. Case Report: We present a rare case of a 17 year-old male diagnosed with subcutaneous pannicultic T-cell lymphoma manifesting with prolonged fever, weight loss, and multiple subcutaneous nodules. He also presented with extra-cutaneous manifestations of facial edema, pleural effusion and ascites, lymph node enlargement, hepatosplenomegaly with jaundice and pancytopenia. Conclusion and Summary: Subcutaneous Panniculitic T-Cell Lymphoma may present with an unusual finding of facial edema, ascites and pleural effusion, lymph node enlargement, hepatosplenomegaly with jaundice and pancytopenia alongside skin manifestations of subcutaneous panniculitis. HPS may complicate the course, treatment decisions and outcome of the disease.


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