Córdoba Díaz de Laspra E, Calleja J L, Hernando E, Lahuerta L, Ceballos C, Cardiel M J, del Río Marco F, Ferreira Montero V
Department of General Surgery, Miguel Servet Hospital, Zaragoza, Spain.
J R Coll Surg Edinb. 1997 Oct;42(5):355-8.
We report a new case of primary malignant fibrous histiocytoma of the jejunum. Malignant fibrous histiocytoma (MFH) occurs most commonly in the extremities and trunk, but rarely in visceral organs. However, only eight cases of primary tumours involving the small intestine, including the present, have been described. This case report documents the appearance of malignant fibrous histiocytoma as a primary lesion of the intestinal wall in a patient with a 2-month history of dyspepsia, weight loss and unspecific abdominal pain. The final diagnosis was based on the pathological report of the surgical specimen. Emphasis is placed on the clinical signs, radiological studies and pathological findings. The literature on MFH of the jejunum is also reviewed. Malignant fibrous histiocytoma is considered an aggressive tumour, and the treatment of choice is complete surgical excision. Adjuvant chemotherapy or radiation is recommended mainly in those patients in whom there is vascular or lymphatic infiltration.
我们报告一例空肠原发性恶性纤维组织细胞瘤的新病例。恶性纤维组织细胞瘤(MFH)最常发生于四肢和躯干,很少发生于内脏器官。然而,包括本病例在内,仅有8例累及小肠的原发性肿瘤被描述。本病例报告记录了一名有2个月消化不良、体重减轻和非特异性腹痛病史的患者,恶性纤维组织细胞瘤表现为肠壁的原发性病变。最终诊断基于手术标本的病理报告。重点介绍了临床体征、影像学检查和病理结果。同时也回顾了关于空肠MFH的文献。恶性纤维组织细胞瘤被认为是一种侵袭性肿瘤,治疗的首选方法是完整的手术切除。主要推荐对那些有血管或淋巴浸润的患者进行辅助化疗或放疗。