Hauser H, Beham A, Uranüs S, Frühwirth H, Lederer A, Klimpfinger M
Universitätsklinik für Chirurgie, Graz.
Z Gastroenterol. 1993 Dec;31(12):735-8.
Malignant fibrous histiocytoma (MFH) is a tumor most frequently occurring in lower and upper extremities and in retroperitoneum. This paper presents the extremely rare case of a 55-year-old male patient with a MFH of storiform pleomorphic subtype originating from the mesentery. Sonography, computed tomography as well as endoscopy and ERCP did not reveal the diagnosis. Finally the tumor was diagnosed by laparoscopy with biopsy and histological examination. Two months after diagnosis of the tumor the patient died of bronchopneumony and heart failure contracted during a generalisation of MFH.
恶性纤维组织细胞瘤（MFH）是一种最常发生于下肢、上肢及腹膜后的肿瘤。本文报告了一例极为罕见的病例，一名55岁男性患者，患有起源于肠系膜的席纹状多形性亚型MFH。超声检查、计算机断层扫描以及内镜检查和内镜逆行胰胆管造影（ERCP）均未明确诊断。最终通过腹腔镜活检及组织学检查确诊了该肿瘤。肿瘤确诊两个月后，患者死于支气管肺炎及MFH播散期间并发的心力衰竭。
