Hepatosplenic T-Cell Lymphoma Mimicking Acute Onset of Cholestatic Hepatitis in a Young Immunocompetent Man: A Case Report

نویسندگان

چکیده

We herein report a case of hepatosplenic T-cell lymphoma (HSTCL) incidentally found in 30-year-old man who came to the emergency department after an ankle trauma. At admission, laboratory tests revealed abnormal liver enzymes and pancytopenia, imaging showed mild hepatosplenomegaly. During hospitalization, patient’s clinical condition worsened rapidly, with concomitant increase cholestatic enzymes, severe jaundice, worsening pancytopenia. Causes injury, including many infectious diseases, were explored until diagnosis HSTCL was made by bone marrow biopsies. Subsequently, patient underwent six cycles chemotherapy CHOP (cyclophosphamide, hydroxydaunorubicin, oncovin prednisone or prednisolone) regimen one Hyper-CVAD (fractionated cyclophosphamide, vincristine, doxorubicin, dexamethasone) but, despite this aggressive treatment, died due disease progression 2 months diagnosis. This rare should be considered diagnostic workup acute hepatitis presenting hepatosplenomegaly cytopenia.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Primary cutaneous CD30+T cell lymphoma: A case report

Primary cutaneous CD30+ T cell lymphoma is rare lymphoma originally in and confined to the skin. These lymphomas usually present as a large solitary and often ulcerated nodule. Its prognosis is a good and has a good response to radiotherapy. We report a 34- year- old man who had primary cutaneous CD30+T cell lymphoma on his face, which presented as an ulcerated nodule.

متن کامل

Hepatosplenic T-cell lymphoma: A case series.

Hepatosplenic T-cell lymphoma (HSTCL) is a rare type of Non-Hodgkin Lymphoma (NHL), grouped under the mature or peripheral T-cell lymphomas. It is characterised by extranodal infiltration and proliferation of malignant T-cells within the sinusoids of the liver, sinuses and red pulp of the spleen, and the bone marrow. The tumour cells express CD2 and CD3, but are CD4, CD5 and CD8 negative and ex...

متن کامل

Hemophagocytic lymphohistiocytosis associated with hepatosplenic T-cell lymphoma: case report

Hepatosplenic T-cell lymphoma (HSTCL) is a rare non-Hodgkin lymphoma, marked by liver, spleen, and bone marrow sinusoidal infiltration, with an aggressive clinical course, which represents a difficult diagnostic task for clinicians and pathologists. Another equally severe and challenging condition is the hemophagocytic lymphohistiocytosis (also called hemophagocytic syndrome [HS]), which is oft...

متن کامل

Hepatosplenic T-cell Lymphoma: Case Report & Literature Review

Hepatosplenic T-cell lymphoma (HSTCL) was first described as a distinct clinicopathologic entity in 1990. HSTCL is more common among young males in their teenage years and in young adulthood. It is an aggressive tumor. Our patient presented with pancytopenia, hepatosplenomegaly but no lymphadenopathy. The key role for diagnosis was through identifying of double negative CD4, CD8 negative lympho...

متن کامل

Diffuse normolipemic plane Xanthoma in adult T-cell lymphoma/leukemia: A case report

Diffuse normolipemic plane xanthoma is a rare disorder often seen as a para-neoplastic manifestation accompanied with gammopathies and hematologic disorders. In this report, a 44-year-old man is presented who was referred to us due to developing erythematous papules on the hands and yellow patches on different parts of the body. Based on cell blood count, peripheral blood smear and positive ant...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Gastroenterology Insights

سال: 2022

ISSN: ['2036-7422', '2036-7414']

DOI: https://doi.org/10.3390/gastroent13030026