[通过外显子组分析发现与脾边缘区淋巴瘤同源的组织细胞肉瘤]。

Daiki Komata, Mutsumi Takahata, Yoshinori Makino, Takashi Ishio, Hiroshi Iwasaki, Shin Ichihara, Masumi Tsuda, Shinya Tanaka, Makoto Ibata
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摘要

组织细胞肉瘤(HS)是一种罕见的侵袭性血液恶性肿瘤,据报道可继发于B细胞淋巴瘤。我们报告了一例继发于脾边缘区淋巴瘤(SMZL)并伴有自身免疫性溶血性贫血(AIHA)的组织细胞肉瘤病例,患者是一名64岁的男性。他因贫血转诊至我科,被诊断为 AIHA。在开始接受泼尼松龙治疗后,他的血检中出现了非典型淋巴细胞,骨髓活检显示有B细胞淋巴瘤侵犯。CT 扫描显示脾脏肿大和胰腺肿块,确诊为 SMZL。患者接受了苯达莫司汀和利妥昔单抗化疗,贫血和脾肿大迅速得到改善,非典型淋巴细胞也有所减少。然而,随着胰腺肿块的增大,他出现了左腰背部疼痛,并突然死于急性肾衰竭。尸检显示,肿瘤侵犯了包括胰腺在内的多个器官,免疫组化显示 CD163 阳性,因此诊断为 HS。此外,SMZL和HS标本的IgH基因重组均呈阳性,外显子组分析显示包括CARD11在内的226个基因存在遗传异常,这表明SMZL和HS具有相同的起源。
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[Histiocytic sarcoma derived from the same origin as splenic marginal zone lymphoma revealed by exome analysis].

Histiocytic sarcoma (HS) is a rare aggressive hematological malignancy reported to occur secondary to B cell lymphoma. We report a case of HS secondary to splenic marginal zone lymphoma (SMZL) complicated by autoimmune hemolytic anemia (AIHA) in a 64-year-old man. He was referred to our department with anemia and was diagnosed as having AIHA. After starting treatment with prednisolone, atypical lymphocytes appeared in his blood tests, and a bone marrow biopsy revealed invasion by B cell lymphoma. A CT scan showed splenomegaly and a pancreatic mass, which confirmed the diagnosis of SMZL. The patient received bendamustine and rituximab as chemotherapy, which rapidly improved the anemia and splenomegaly and reduced atypical lymphocytes. However, left lumbar back pain appeared along with an increase in the pancreatic mass, and he died suddenly of acute renal failure. An autopsy revealed that the tumor had invaded several organs including the pancreas, and immunohistochemistry was positive for CD163, leading to the diagnosis of HS. Furthermore, the specimens of SMZL and HS were positive for IgH gene reconstitution, and exome analysis showed genetic abnormalities in 226 genes including CARD11, suggesting that the SMZL and HS had the same origin.

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