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原发性鼻窦黏液纤维肉瘤:5 例临床病理研究及文献复习。

Primary sinonasal myxofibrosarcoma: a clinicopathological study of five cases and review of the literature.

机构信息

Department of Pathology, Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, OH, USA.

Department of Anatomic Pathology, Middlemore Hospital, Counties Manukau District Health Board, Auckland, New Zealand.

出版信息

Pathology. 2022 Feb;54(1):63-70. doi: 10.1016/j.pathol.2021.04.009. Epub 2021 Jul 21.

Abstract

Myxofibrosarcoma is a malignant pleomorphic fibroblastic sarcoma with variably myxoid stroma, and is characterised by a distinctive curvilinear vascular pattern. In the head and neck area, myxofibrosarcoma is extremely rare, with only a handful of case reports in the literature to date. We report the first case series of primary sinonasal myxofibrosarcoma across two institutions. Among the five cases (2 female, 3 males, aged 52-82 years old), four arose from the maxillary sinus and one from the sphenoid sinus. Four patients received surgical resection and three with adjuvant radiotherapy. The tumours ranged from 2.9 to 5.6 cm in greatest dimensions. All tumours demonstrated extensive myxoid stroma (>50% myxoid component) with a characteristic curvilinear, elongated, thin-walled vasculature with perivascular condensation of tumour cells. All but one were classified as intermediate to high grade myxofibrosarcoma. Among the four patients with follow-up information, three reported no local recurrence or distal metastasis, and one had local recurrence. Myxofibrosarcoma should be included in the differential diagnosis of sinonasal tumours with a pleomorphic spindle cell morphology and a 'null' immunophenotype.

摘要

黏液纤维肉瘤是一种具有不同程度黏液样基质的恶性多形性成纤维细胞肉瘤,其特征是具有独特的曲线状血管模式。在头颈部,黏液纤维肉瘤极为罕见,目前文献中仅有少数病例报告。我们报告了两个机构的首例原发性鼻腔鼻窦黏液纤维肉瘤病例系列。在 5 例患者中(2 例女性,3 例男性,年龄 52-82 岁),4 例起源于上颌窦,1 例起源于蝶窦。4 例患者接受了手术切除,3 例患者接受了辅助放疗。肿瘤最大直径为 2.9 至 5.6 厘米。所有肿瘤均表现为广泛的黏液样基质(>50%黏液样成分),具有特征性的曲线状、细长、薄壁血管,伴有血管周围肿瘤细胞凝聚。除 1 例外,其余均被归类为中至高分化黏液纤维肉瘤。在有随访信息的 4 例患者中,3 例报告无局部复发或远处转移,1 例有局部复发。黏液纤维肉瘤应包括在具有多形性梭形细胞形态和“空”免疫表型的鼻窦肿瘤的鉴别诊断中。

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