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进行性骨化性纤维发育不良:一种独特的软组织骨形成病变。

Fibrodysplasia ossificans progressiva: a distinctive bone-forming lesion of the soft tissue.

作者信息

Cramer S F, Ruehl A, Mandel M A

出版信息

Cancer. 1981 Aug 15;48(4):1016-21. doi: 10.1002/1097-0142(19810815)48:4<1016::aid-cncr2820480428>3.0.co;2-y.

Abstract

A 3-month-old white female presented with a bone-forming lesion of the soft tissue of the left cheek. Skeletal survey revealed numerous associated radiographic abnormalities, predominantly involving the phalanges. Mineral metabolism and endocrine function were within normal limits. Multiple operations were performed over a 17-year period for palliation of sequelae arising from inability to open the mouth due to ankylosis of the temporomandibular joint by the progressively ossifying lesion. Histologically, the pathologic material had features resembling those of periosteal grafts, with all stages of membranous bone formation and a tendency for more mature lesions later in the course. .The clinico-pathologic features are those of fibrodysplasia ossificans progressiva (FOP). The differential diagnosis of this rare condition from other bone-forming lesions of the soft tissue such as myositis ossificans, extra-skeletal osteosarcoma and osseous metaplasia is discussed.

摘要

一名3个月大的白人女性因左脸颊软组织出现骨形成性病变前来就诊。骨骼检查发现了许多相关的影像学异常,主要累及指骨。矿物质代谢和内分泌功能均在正常范围内。在17年的时间里,由于进行性骨化性病变导致颞下颌关节强直而无法开口,为此进行了多次手术以缓解后遗症。组织学上,病理材料具有类似于骨膜移植的特征,具有膜性骨形成的所有阶段,且病程后期有形成更成熟病变的倾向。临床病理特征符合进行性骨化性纤维发育不良(FOP)。本文讨论了这种罕见疾病与其他软组织骨形成性病变(如骨化性肌炎、骨外骨肉瘤和骨化生)的鉴别诊断。

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