M. Indu, Ravindra Kanthaliya, Swati Jami, Brijesh Sharma, D. S. Chauhan, Jyoti Garg, Jyotsana P Lalita
{"title":"Myelofibrosis secondary to Hodgkin’s lymphoma: A case report","authors":"M. Indu, Ravindra Kanthaliya, Swati Jami, Brijesh Sharma, D. S. Chauhan, Jyoti Garg, Jyotsana P Lalita","doi":"10.4103/ijh.ijh_37_23","DOIUrl":null,"url":null,"abstract":"A 23-year-old male was misdiagnosed as a case of tubercular lymphadenitis based on fever with B-symptoms and finding of epithelioid granuloma on fine-needle aspiration of mesenteric lymph node and was started on antitubercular treatment from an outside hospital. Since the patient had progression of symptoms, we re-evaluated the case. Contrast-enhanced computed tomography showed multiple conglomerated necrotic cervical, peritoneal lymph nodes, hepatosplenomegaly, and multiple mixed sclerotic lytic lesions in multiple vertebral bodies and pelvis. An excision lymph node biopsy was suggestive of a nodular sclerosis variant of Hodgkin’s lymphoma. A bone marrow study was performed subsequent to new-onset bicytopenia. Bone marrow aspiration was dry and bone marrow biopsy showed myelofibrosis. Thus, a diagnosis of myelofibrosis secondary to Hodgkin’s lymphoma was made.","PeriodicalId":53847,"journal":{"name":"Iraqi Journal of Hematology","volume":null,"pages":null},"PeriodicalIF":0.1000,"publicationDate":"2023-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iraqi Journal of Hematology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijh.ijh_37_23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
A 23-year-old male was misdiagnosed as a case of tubercular lymphadenitis based on fever with B-symptoms and finding of epithelioid granuloma on fine-needle aspiration of mesenteric lymph node and was started on antitubercular treatment from an outside hospital. Since the patient had progression of symptoms, we re-evaluated the case. Contrast-enhanced computed tomography showed multiple conglomerated necrotic cervical, peritoneal lymph nodes, hepatosplenomegaly, and multiple mixed sclerotic lytic lesions in multiple vertebral bodies and pelvis. An excision lymph node biopsy was suggestive of a nodular sclerosis variant of Hodgkin’s lymphoma. A bone marrow study was performed subsequent to new-onset bicytopenia. Bone marrow aspiration was dry and bone marrow biopsy showed myelofibrosis. Thus, a diagnosis of myelofibrosis secondary to Hodgkin’s lymphoma was made.
一名 23 岁的男性因发热伴 B 型症状,以及肠系膜淋巴结细针穿刺发现上皮样肉芽肿而被误诊为结核性淋巴结炎,并开始在外院接受抗结核治疗。由于患者症状加重,我们对病例进行了重新评估。对比增强计算机断层扫描显示,患者颈部、腹膜淋巴结多发聚集性坏死,肝脾肿大,多个椎体和骨盆多发混合性硬化性淋巴结病变。切除淋巴结活检提示为霍奇金淋巴瘤的结节硬化变异型。由于新出现的全血细胞减少症,患者接受了骨髓检查。骨髓抽吸呈干性,骨髓活检显示骨髓纤维化。因此,诊断为继发于霍奇金淋巴瘤的骨髓纤维化。