Pednekar Sangeeta, Morge Vinayak, Rawal Shailesh, Korivi Deepa, Ramteke Vishal, Naik Kiran
Department of Medicine, LTM Medical College and LTMG Hospital, Sion, Mumbai 400022.
J Assoc Physicians India. 2011 Oct;59:667-8.
We report a case of 18 year old male who presented with hepatosplenomegaly, anemia and thrombocytopenia. His complete hemogram, peripheral smear, bone marrow studies were inconclusive. On immunophenotyping he was diagnosed as "Hepatosplenic gamma delta (gammadelta) T cell lymphoma" which is a very rare variety of T cell lymphoma. Less than 100 cases have been described in the literature since the entity was first described in 1990.
我们报告一例18岁男性患者，其表现为肝脾肿大、贫血和血小板减少。他的全血细胞计数、外周血涂片、骨髓检查结果均不明确。经免疫表型分析，他被诊断为“肝脾γδ（伽马德尔塔）T细胞淋巴瘤”，这是一种非常罕见的T细胞淋巴瘤。自1990年首次描述该实体以来，文献中报道的病例不足100例。
