翻訳と辞書 |
Fetal rhabdomyoma : ウィキペディア英語版 | Fetal rhabdomyoma
Rhabdomyoma is a benign mesenchymal tumor of skeletal muscle, separated into two major categories based on site: Cardiac and extracardiac. They are further separated by histology: fetal (myxoid and cellular), juveline (intermediate), and adult types. Genital types are recognized, but are often part of either the fetal or juveline types. The fetal type is thought to recapitulate immature skeletal muscle at about week six to ten of gestational development. == Signs and symptoms == Most fetal rhabdomyomas are tumors that develop in the head and neck or in the genital region.〔Lapner PC, Chou S, Jimenez C. Perianal fetal rhabdomyoma: case report. Pediatr Surg Int 1997;12(7):544-7.〕 There are a number of cases which have been seen in association with Gorlin syndrome.〔Watson J, Depasquale K, Ghaderi M, Zwillenberg S. Nevoid basal cell carcinoma syndrome and fetal rhabdomyoma: a case study. Ear Nose Throat J 2004;83(10):716-8.〕〔Hardisson D, Jimenez-Heffernan JA, Nistal M, Picazo ML, Tovar JA, Contreras F. Neural variant of fetal rhabdomyoma and naevoid basal cell carcinoma syndrome. Histopathology 1996;29(3):247-52.〕 However, cardiac myxomas are known to be associated with tuberous sclerosis.
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Fetal rhabdomyoma」の詳細全文を読む
スポンサード リンク
翻訳と辞書 : 翻訳のためのインターネットリソース |
Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.
|
|