MEN1 Syndrome and Hibernoma: An Uncommonly Recognised Association?

被引：5

作者：

Hedayati, Venus ^{[1
]}

Thway, Khin ^{[1
]}

Thomas, J. Meirion ^{[1
]}

Moskovic, Eleanor ^{[1
]}

机构：

[1] Royal Marsden Hosp, FulhamRd, London SW3 6JJ, England

来源：

CASE REPORTS IN MEDICINE | 2014年 / 2014卷

关键词：

D O I：

10.1155/2014/804580

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

MEN1 syndrome is known to classically result in parathyroid, pituitary, and pancreatic islet cell tumours. However, the potential association of MEN1 syndrome with hibernoma, a benign tumour with differentiation towards brown fat, is far less well known, despite their genetic profile both being linked to deletion of the MEN1 gene. Herein, we describe a case with its key radiological and pathological findings.

引用

页数：4

共 50 条

[21] Case problem: Nutrition support in MEN1 syndrome
Trombley, LE
JOURNAL OF THE AMERICAN DIETETIC ASSOCIATION, 2001, 101 (12) : 1475 - 1477
[22] WGS confirms the diagnosis of MEN1 syndrome in a suspected pediatric MEN1 case from Qatar, a case report
Al-Barazenji, Tara
Mohammed, Idris
Chirayath, Shiga
Al-Shafai, Mashael
HORMONE RESEARCH IN PAEDIATRICS, 2024, 97 : 615 - 615
[23] Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma
Nord, Karolin H.
Magnusson, Linda
Isaksson, Margareth
Nilsson, Jenny
Lilljebjorn, Henrik
Domanski, Henryk A.
Kindblom, Lars-Gunnar
Mandahl, Nils
Mertens, Fredrik
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (49) : 21122 - 21127
[24] Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation
Hasani-Ranjbar, Shirin
Rahmanian, Masoud
Ebrahim-Habibi, Azadeh
Soltani, Akbar
Soltanzade, Akbar
Mahrampour, Elnaz
Amoli, Mahsa M.
FAMILIAL CANCER, 2014, 13 (02) : 267 - 272
[25] Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation
Shirin Hasani-Ranjbar
Masoud Rahmanian
Azadeh Ebrahim-Habibi
Akbar Soltani
Akbar Soltanzade
Elnaz Mahrampour
Mahsa M. Amoli
Familial Cancer, 2014, 13 : 267 - 272
[26] Novel association of MEN1 gene mutations with parathyroid carcinoma
Cinque, Luigia
Sparaneo, Angelo
Cetani, Filomena
Coco, Michelina
Clemente, Celeste
Chetta, Massimiliano
Balsamo, Teresa
Battista, Claudia
Sanpaolo, Eliana
Pardi, Elena
D'Agruma, Leonardo
Marcocci, Claudio
Maiello, Evaristo
Hendy, Geoffrey N.
Cole, David E. C.
Scillitani, Alfredo
Guarnieri, Vito
ONCOLOGY LETTERS, 2017, 14 (01) : 23 - 30
[27] Mutational spectrum of MEN1 and MEN2 syndrome in Croatian patients
Sorgic, Ana Merkler
Ljubic, Hana
Barisic, Ana Acman
Caban, Domagoj
Kusacic-Kuna, Sanja
Krnic, Nevena
Kastelan, Darko
Rako, Ivana
EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 131 - 132
[28] MEN1 at work
Voigt, K
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2000, 108 (05) : 327 - 327
[29] MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism
Vince Kornél Grolmusz
Katalin Borka
Annamária Kövesdi
Kinga Németh
Katalin Balogh
Csaba Dékány
András Kiss
Anna Szentpéteri
Beatrix Sármán
Anikó Somogyi
Éva Csajbók
Zsuzsanna Valkusz
Miklós Tóth
Péter Igaz
Károly Rácz
Attila Patócs
Virchows Archiv, 2017, 471 : 401 - 411
[30] MEN1 syndrome - Data from a single referral center
Papadopoulou-Marketou, N.
Alexandraki, K.
Panagaki, M.
Tsoli, M.
JOURNAL OF NEUROENDOCRINOLOGY, 2023, 35 : 103 - 103

← 1 2 3 4 5 →