Primary Cutaneous Neuroendocrine Tumor of the Vulva: A Case Report

Autor: Shaimaa Al-Janabi, Jenneke C. Kasius, Elisabeth H. Jaspars, Malou L.H. Snijders

Publikováno v: International Journal of Gynecological Pathology, 42(3), 278-281. Lippincott Williams and Wilkins
International journal of gynecological pathology, 42(3), 278-281. Lippincott Williams and Wilkins
Al-Janabi, S, Kasius, J C, Jaspars, E H & Snijders, M L H 2023, ' Primary Cutaneous Neuroendocrine Tumor of the Vulva : A Case Report ', International Journal of Gynecological Pathology, vol. 42, no. 3, pp. 278-281 . https://doi.org/10.1097/PGP.0000000000000919

Primary cutaneous neuroendocrine tumors (CNET) are extremely rare. Only a few cases have been reported so far. CNET have an indolent clinical course and usually presents as a single flesh-colored nodule with a predilection for the scalp and trunk in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cad7843486bf98304d25ae7aac69f50c
https://research.vumc.nl/en/publications/835209a4-f7ca-496b-bd6b-4fc1c2487aed

Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families

Autor: Elisabeth H Jaspars, N.C.T. van Grieken, M. B. A. van Doorn, Edward M Leter, Ernie M.H.F. Bongers, Paul C Johannesma, Pieter E. Postmus, Lieke Gijezen, J-H T. M. van Waesberghe, Theo M. Starink, M.A.M. van Steensel, Arjan C. Houweling, Rogier A. Oldenburg, R.J.A. Van Moorselaar, Marianne A. Jonker, T. A. M. van Os, Johan J.P. Gille, K. Y. van Spaendonck-Zwarts, M. M. de Jong, Fred H. Menko

Publikováno v: British Journal of Cancer, 105(12), 1912-1919. Nature Publishing Group
Houweling, A C, Gijezen, L M, Jonker, M A, van Doorn, M B A, Oldenburg, R A, van Spaendonck-Zwarts, K Y, Leter, E M, van Os, T A M, van Grieken, N C T, Jaspars, E H, de Jong, M M, Bongers, E M H F, Johannesma, P C, Postmus, P E, van Moorselaar, R J A, van Waesberghe, J H T M, Starink, T M, van Steensel, M A M, Gille, J J P & Menko, F H 2011, ' Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families ', British Journal of Cancer, vol. 105, no. 12, pp. 1912-1919 . https://doi.org/10.1038/bjc.2011.463
British Jounal of Cancer, 105(12), 1912-1919. Nature Publishing Group
British Journal of Cancer
British journal of cancer, 105(12), 1912-1919. Nature Publishing Group

Background: Birt-Hogg-Dubé (BHD) syndrome is an autosomal dominant condition caused by germline FLCN mutations, and characterised by fibrofolliculomas, pneumothorax and renal cancer. The renal cancer risk, cancer phenotype and pneumothorax risk of B

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee60ff288397312c36a9973e0efd5722
https://doi.org/10.1038/bjc.2011.463

Russell bodies in a skin biopsy: a case report

Autor: Lawrence Rozendaal, Elisabeth H Jaspars, Paul van der Valk, Joanne Verheij

Publikováno v: Journal of medical case reports, 3:108. BioMed Central
Verheij, J, Jaspars, E H, van der Valk, P & Rozendaal, L 2009, ' Russell bodies in a skin biopsy: a case report ', Journal of medical case reports, vol. 3, 108 . https://doi.org/10.1186/1752-1947-3-108
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 3, Iss 1, p 108 (2009)

Introduction The presence of eosinophilic bodies in a skin biopsy can be found in a variety of situations and this may present a challenge to the pathologist. The differential diagnosis of these eosinophilic structures include microorganisms such as

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44ecca1784ae3173024b9a8a9aca3c7f
https://doi.org/10.1186/1752-1947-3-108

Familial multiple discoid fibromas: A look-alike of Birt-Hogg-Dubé syndrome not linked to the FLCN locus

Autor: Martijn B.A. van Doorn, Johan J.P. Gille, Arjan C. Houweling, Fred H. Menko, Theo M. Starink, P.C. Johannesma, Quinten Waisfisz, R. Jeroen A. van Moorselaar, Jan Hein T.M. van Waesberghe, Martijn H. Ploeger, Piet E. Postmus, Edward M Leter, Marieke T. Kramer, Elisabeth H. Jaspars

Publikováno v: Starink, T M, Houweling, A C, van Doorn, M B A, Leter, E M, Jaspars, E H, van Moorselaar, R J A, Postmus, P E, Johannesma, P C, van Waesberghe, J H T M, Ploeger, M H, Kramer, M T, Gille, J J P, Waisfisz, Q & Menko, F H 2012, ' Familial multiple discoid fibromas: A look-alike of Birt-Hogg-Dube syndrome not linked to the FLCN locus ', Journal of the American Academy of Dermatology, vol. 66, no. 2, pp. 259-263 . https://doi.org/10.1016/j.jaad.2010.11.039
Journal of the American Academy of Dermatology, 66(2), 259-263. Mosby Inc.

Background Previously, we proposed that familial multiple trichodiscomas (OMIM 190340) is distinct from Birt-Hogg-Dube syndrome (BHD) (OMIM #135150). BHD is characterized by multiple fibrofolliculomas/trichodiscomas, lung cysts, pneumothorax, and ren

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e43a99395dd3de63adb6abf5bbeb1ec7
https://doi.org/10.1016/j.jaad.2010.11.039