1例未经治疗的胰腺头区髓系肉瘤:一例自体病例的AML亚型诊断过程。

IF 0.7 Q4 PATHOLOGY
Case Reports in Pathology Pub Date : 2021-12-21 eCollection Date: 2021-01-01 DOI:10.1155/2021/7439148
Yuki Fukumura, Gentaro Taniguchi, Ai Koyanagi, Yuki Horiuchi, Tomonori Ochiai, Yoko Tabe, Katsuhiro Sano, Yifare Maimaitiaili, Naomi Otsuji, Karin Ashizawa, Takashi Yao
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引用次数: 1

摘要

本研究描述了一个70岁男性胰腺/胰腺周围髓样肉瘤的尸检病例,最初表现为梗阻性黄疸。病理上,主要在胰头、胰周淋巴结、脾、双侧肺和骨髓可见含有不典型核的圆形细胞弥漫性浸润,细胞核分裂明显。免疫组化结果显示,肿瘤细胞CD20、CD79a、CD3、CD5、c-kit、CD34和TdT呈阴性,髓过氧化物酶、CD33、CD68和CD163呈阳性。外周血流式细胞术显示单核细胞亚群中CD11c低表达和CD56异常表达。外周血涂片显示单核细胞增多,中性粒细胞和单核细胞异型性增多,血小板和红细胞增多。因此,我们认为骨髓肉瘤是由慢性髓细胞白血病的急性转化而来的。髓样肉瘤是一种髓外肿块形成的血液恶性肿瘤,很难诊断,特别是当最初表现为胰腺肿块时。然而,早期诊断对于适当的治疗很重要。虽然由于患者病情严重,无法进行骨髓检查,但尸检获得的病理标本有助于对患者的白血病进行分型。本病例的免疫组织化学特征值得注意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Case of Untreated Myeloid Sarcoma of the Pancreas Head Region: Diagnostic Process of AML Subtyping in an Autoptic Case.

A Case of Untreated Myeloid Sarcoma of the Pancreas Head Region: Diagnostic Process of AML Subtyping in an Autoptic Case.

A Case of Untreated Myeloid Sarcoma of the Pancreas Head Region: Diagnostic Process of AML Subtyping in an Autoptic Case.

A Case of Untreated Myeloid Sarcoma of the Pancreas Head Region: Diagnostic Process of AML Subtyping in an Autoptic Case.
This study describes an autopsy case of pancreatic/peripancreatic myeloid sarcoma in a 70-year-old man, initially presenting with obstructive jaundice. Pathologically, diffuse infiltration of round cells containing atypical nuclei with marked cleavage was observed mainly in the pancreas head, peripancreatic lymph nodes, spleen, bilateral lung, and bone marrow. Immunohistochemically, the tumor cells were negative for CD20, CD79a, CD3, CD5, c-kit, CD34, and TdT and positive for myeloperoxidase, CD33, CD68, and CD163. Flow cytometry of the peripheral blood showed underexpression of CD11c and aberrant expression of CD56 in the monocyte subset. The peripheral blood smear showed an increase in monocytes and atypia in neutrophils and monocytes, as well as enlarged platelets and polychromatic erythroblasts. Hence, it was suggested that the myeloid sarcoma was derived from the acute transformation of chronic myelomonocytic leukemia. Myeloid sarcoma is an extramedullary-mass-forming hematologic malignancy that is difficult to diagnose, especially when the initial presentation is a pancreatic mass. However, early diagnosis is important for appropriate therapy. Although bone marrow examination could not be performed because of the patients' severe condition, the pathological specimen obtained with autopsy helped subtype the patient's leukemia. The immunohistochemical features of this case merit attention.
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