Dysplastic Megakaryocytes in a Gallbladder Neck Lymph Node in a Patient With Essential Thrombocythemia: A Case Report.

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2026-03-05 eCollection Date: 2026-01-01 DOI:10.1155/crh/5591025
Mahi Balcı
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Abstract

A woman in her 60s with a known history of JAK2-positive essential thrombocythemia presented with a one-week history of jaundice. Laboratory testing revealed elevated bilirubin and alkaline phosphatase levels. Abdominal ultrasonography identified a 1-cm gallstone, and laparoscopic cholecystectomy was performed. Histopathological evaluation revealed chronic cholecystitis along with a 5-mm lymph node in the gallbladder neck harboring atypical megakaryocytes with multinucleation and nuclear lobulation. Immunohistochemistry confirmed megakaryocytic origin with strong positivity for CD61 and supportive positivity for Factor VIII, while epithelial and lymphoid markers were negative, ruling out metastatic carcinoma or lymphoma. This case underscores the rare involvement of lymph nodes by dysplastic megakaryocytes in essential thrombocythemia and highlights the importance of considering hematologic malignancies in the differential diagnosis of lymphadenopathy.

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原发性血小板增多症患者胆囊颈淋巴结巨核细胞发育异常1例报告。
60多岁女性,已知jak2阳性原发性血小板增多症病史,有一周黄疸病史。实验室检测显示胆红素和碱性磷酸酶水平升高。腹部超声检查发现1厘米胆结石,行腹腔镜胆囊切除术。组织病理学检查显示慢性胆囊炎伴胆囊颈5毫米淋巴结,内有非典型巨核细胞,伴多核和核分叶。免疫组织化学证实巨核细胞来源,CD61强阳性,因子VIII支持阳性,而上皮和淋巴细胞标志物阴性,排除转移癌或淋巴瘤。本病例强调了原发性血小板增多症中罕见的增生异常巨核细胞累及淋巴结,并强调了在鉴别诊断淋巴结病时考虑血液恶性肿瘤的重要性。
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审稿时长
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