MR findings of uterine PEComa in patients with tuberous sclerosis: report of two cases

Naoko Nishio, Aki Kido*, Sachiko Minamiguchi, Kayo Kiguchi, Yasuhisa Kurata, Kyoko Kameyama Nakao, Ryo Kuwahara, Ryo Yajima, Satoshi Otani, Masaki Mandai, Kaori Togashi, Manabu Minami

*この論文の責任著者

研究成果: ジャーナルへの寄稿学術論文査読

12 被引用数 (Scopus)

抄録

Tuberous sclerosis complex (TSC), a rare autosomal dominant neurocutaneous disorder, is characterized by the presence of benign congenital tumors in multiple organs. Neoplasms with perivascular epithelioid cell differentiation (PEComas), including angiomyolipoma (AML) and lymphangioleiomyomatosis (LAM), can occur in association with TSC. This report describes two cases of uterine PEComas presenting characteristic MR imaging features reflecting pathological findings. From MR images, both cases showed single or multiple large, irregularly shaped or lobulated hemorrhagic lesions within the myometrium. They differed from typical adenomyotic cysts in their large size and irregular margins. Histopathologic analysis revealed that the hemorrhage was caused by adenomyosis and tumor cells that proliferated in surrounding stroma of the hemorrhagic lesions, compatible with PEComas. Microscopic observation revealed an infiltrative growth pattern of PEComas, with small nodules formed. The tumor lesions, however, were difficult to detect on MR images. The myometrium showed normal appearance on both T1-weighted and T2-weighted images in both cases. We speculate that PEComas may infiltrate extensively into the myometrium even when the myometrium shows almost normal radiologic appearance.

本文言語英語
ページ(範囲)1256-1260
ページ数5
ジャーナルAbdominal Radiology
44
4
DOI
出版ステータス出版済み - 2019/04/01

ASJC Scopus 主題領域

  • 放射線技術および超音波技術
  • 放射線学、核医学およびイメージング
  • 消化器病学
  • 泌尿器学

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