Leiomyomatosis developed in a patient of neurofibromatosis type 1 with fumarate hydratase gene mutation-Reference-Cited by-同舟云学术

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Leiomyomatosis developed in a patient of neurofibromatosis type 1 with fumarate hydratase gene mutation

Published:2019-08-16 Issue:12 Volume:46 Page:
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Otake Eika¹,Hayama Koremasa¹^ORCID,Fujita Hideki¹,Shinkuma Satoru²³^ORCID,Shimizu Hiroshi²,Terui Tadashi¹

Affiliation:

1. Division of Cutaneous Science Department of Dermatology Nihon University School of Medicine Tokyo Japan

2. Department of Dermatology Hokkaido University Graduate School of Medicine Sapporo Japan

3. Division of Dermatology Niigata University Graduate School of Medical and Dental Sciences Niigata Japan

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.15053

Reference5 articles.

1. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

2. Neurofibromatosis type 1-associated tumours: Their somatic mutational spectrum and pathogenesis

3. Gastro-intestinal bleeding caused by leiomyoma of the small intestine in a child with neurofibromatosis

4. Leiomyoma of the bladder in a patient with von Recklinghausen's neurofibromatosis

5. Pelvic mass in von Recklinghausen's neurofibromatosis: diagnostic issues: a case report

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