Kamoshita M, Suzukawa K, Kobayashi T, Hasegawa Y, Satoh Y, Ninomiya H, Nagasawa T, Abe T
Division of Hematology, University of Tsukuba.
Rinsho Ketsueki. 1995 Jan;36(1):59-62.
We reported a case of von Recklinghausen's disease complicated by macroglobulinemia, malignant Schwannoma and pheochromocytoma. A 43-year-old male patient who was diagnosed as von Recklinghausen's disease developed abdominal masses at 5 years after the adrenalectomy for pheochromocytoma. Computed tomography showed multiple heterogeneous tumors in abdominal cavity. Histological examination of resected tumor was compatible with malignant Schwannoma. At the same time, peripheral blood and bone marrow smears showed a large number of plasmacytoid lymphocytes. Immunoelectrophoresis revealed M-protein of IgM, kappa type. He was also diagnosed of coexistence with macroglobulinemia. The chemotherapeutic protocols used were not effective against both malignant Schwannoma and macroglobulinemia. The present case is a rare case of von Recklinghausen's disease associated with triple neoplasms.
我们报告了一例合并巨球蛋白血症、恶性神经鞘瘤和嗜铬细胞瘤的冯雷克林霍增氏病。一名43岁男性患者,被诊断为冯雷克林霍增氏病,在因嗜铬细胞瘤行肾上腺切除术后5年出现腹部肿块。计算机断层扫描显示腹腔内有多个异质性肿瘤。切除肿瘤的组织学检查结果符合恶性神经鞘瘤。同时,外周血和骨髓涂片显示大量浆细胞样淋巴细胞。免疫电泳显示为IgM、κ型M蛋白。他还被诊断为合并巨球蛋白血症。所采用的化疗方案对恶性神经鞘瘤和巨球蛋白血症均无效。本病例是冯雷克林霍增氏病合并三种肿瘤的罕见病例。