Ascites in a patient with hairy cell leukaemia and carcinoma of breast : a diagnostic challenge
Hairy cell leukaemia (HCL) is a rare indolent B-cell lymphoproliferative disorder. We report a diagnostic challenge in detecting the cause of ascites, which is a rare, unique manifestation of HCL. A 72-year-old lady presented with 1-month-history of pain in left upper abdomen and loss of weight. T...
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Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Penerbit Universiti Kebangsaan Malaysia
2021
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Online Access: | http://journalarticle.ukm.my/17418/1/21.pdf http://journalarticle.ukm.my/17418/ https://www.ukm.my/jsm/malay_journals/jilid50bil5_2021/KandunganJilid50Bil5_2021.html |
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Institution: | Universiti Kebangsaan Malaysia |
Language: | English |
Summary: | Hairy cell leukaemia (HCL) is a rare indolent B-cell lymphoproliferative disorder. We report a diagnostic challenge in
detecting the cause of ascites, which is a rare, unique manifestation of HCL. A 72-year-old lady presented with 1-month-history of pain in left upper abdomen and loss of weight. There was hepatomegaly, splenomegaly, bilateral inguinal
lymphadenopathy, anaemia, and lymphocytosis. She was diagnosed as HCL, based on morphology, immunophenotyping
of peripheral blood and bone marrow biopsy examination. In 2009, she was diagnosed as carcinoma of breast when
she presented with a mass in left breast; and she received treatment. For HCL, she received intermittent chemotherapy
(Chlorambucil+ Prednisolone). Her HCL was stable until 2018 when she presented with recurrent ascites which needed
frequent, regular peritoneal paracentesis. Since she had HCL and carcinoma of breast, determining the aetiology of
ascites was challenging. Possible causes of her ascites included metastatic carcinoma of breast, HCL, cirrhosis of liver
with portal hypertension and peritoneal tuberculosis. Cytology of peritoneal fluid showed mature-looking lymphocytes
but no malignant cells. Interestingly, flow cytometry analysis of peritoneal fluid showed the presence of clonal B cell
population with lambda light chain restriction. Therefore, it was concluded that her ascites was a manifestation of
HCL. A few months later, she succumbed to septicaemia. Impact of ascites on disease course of HCL included rapid
disease progression, poor prognosis and shortened survival. We highlight the important role of immunophenotyping
in addition to cytomorphology to guide us in confirming the aetiology of ascites in a patient with haematological and
solid organ malignancies. |
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