Thymic Carcinoid Tumor as Part of a Case of Multiple Endocrine Neoplasia Type I

Thymic Tumors ◽  
2015 ◽  
pp. 59-61
Author(s):  
J. M. Jarry ◽  
M. Labadie ◽  
D. Lefant ◽  
F. Mounios ◽  
M. Bouquet
Keyword(s):  
Carcinoid Tumor ◽  
Multiple Endocrine Neoplasia ◽  
Multiple Endocrine Neoplasia Type ◽  
Type I ◽  
Thymic Carcinoid ◽  
Endocrine Neoplasia ◽  
Endocrine Neoplasia Type ◽  
Thymic Carcinoid Tumor

Cushing's Syndrome Secondary to a Thymic Carcinoid Tumor Due to Multiple Endocrine Neoplasia Type 1

2011 ◽  
Vol 1 (-1) ◽  
pp. 1-16
Author(s):  
Ali A Ghazi ◽  
Azizollah Abbasi Dezfooli ◽  
Farzaneh Mohamadi ◽  
Seyed Vahid Yousefi ◽  
Alireza Amirbaigloo ◽  
...  
Keyword(s):  
Carcinoid Tumor ◽  
Cushing’S Syndrome ◽  
Multiple Endocrine Neoplasia ◽  
Multiple Endocrine Neoplasia Type ◽  
Cushing's Syndrome ◽  
Thymic Carcinoid ◽  
Endocrine Neoplasia ◽  
Endocrine Neoplasia Type ◽  
Thymic Carcinoid Tumor

Cushing Syndrome Secondary to a Thymic Carcinoid Tumor Due to Multiple Endocrine Neoplasia Type 1

2011 ◽  
Vol 17 (4) ◽  
pp. e92-e96 ◽  
Author(s):  
Ali Ghazi ◽  
Azizollah Dezfooli ◽  
Farzaneh Mohamadi ◽  
Seyed Yousefi ◽  
Alireza Amirbaigloo ◽  
...  
Keyword(s):  
Carcinoid Tumor ◽  
Multiple Endocrine Neoplasia ◽  
Multiple Endocrine Neoplasia Type ◽  
Cushing Syndrome ◽  
Thymic Carcinoid ◽  
Endocrine Neoplasia ◽  
Endocrine Neoplasia Type ◽  
Thymic Carcinoid Tumor

scholarly journals A rare case of multiple endocrine neoplasia type 1 initially presenting as an asymptomatic, huge mediastinal mass: case report

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Ji Eun Jun ◽  
You-Cheol Hwang ◽  
Kyu Jeong Ahn ◽  
Ho Yeon Chung ◽  
In-Kyung Jeong
Keyword(s):  
Carcinoid Tumor ◽  
Rare Case ◽  
Multiple Endocrine Neoplasia ◽  
Mediastinal Mass ◽  
Multiple Endocrine Neoplasia Type ◽  
Thymic Carcinoid ◽  
Endocrine Glands ◽  
Endocrine Neoplasia ◽  
Thymic Carcinoid Tumor

Abstract Background Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited syndrome that concurrently involves various endocrine glands. We report a rare case of MEN1 in a 43-year-old man whose first manifestation was an asymptomatic mediastinal mass. Case presentation A 13-cm-sized mediastinal mass was diagnosed as an atypical thymic carcinoid by computed tomography and percutaneous needle biopsy. In addition, hypercalcemia from a left inferior parathyroid hyperplasia, and a non-functioning gastric neuroendocrine tumor seen on esophagogastroduodenoscopy were found. Therefore, the patient was clinically diagnosed with MEN1 syndrome, and underwent surgical resection of thymic carcinoid tumor after pre-operative concurrent chemoradiation therapy to decrease tumor size and volume. Parathyroid lesion and gastric neuroendocrine tumor were also removed. Finally, a MEN1 gene mutation was observed in the patient and his 7-year-old son. Conclusion Despite its rare occurrence, thymic carcinoid tumor should be considered as a MEN1-associated tumor and necessitates screening of other endocrine glands. Thymic carcinoid tumor carries a poor prognosis in patients with MEN1, and thus it needs to be carefully monitored even after radical excision.

scholarly journals Pituitary Adenoma associated with Multiple Endocrine Neoplasia Type I : A Case Report

1997 ◽  
Vol 6 (2) ◽  
pp. 102-106
Author(s):  
Manabu Sasaki ◽  
Masaharu Sato ◽  
Junji Taguchi ◽  
Shigeto Matsumoto ◽  
Toru Sugase ◽  
...  
Keyword(s):  
Case Report ◽  
Pituitary Adenoma ◽  
Multiple Endocrine Neoplasia ◽  
Multiple Endocrine Neoplasia Type ◽  
Type I ◽  
Endocrine Neoplasia ◽  
Endocrine Neoplasia Type

Surgical management of insulinoma associated with multiple endocrine neoplasia type I

1994 ◽  
Vol 18 (4) ◽  
pp. 488-493 ◽  
Author(s):  
Diarmuid S. O'Riordain ◽  
Timothy O'Brien ◽  
Jon A. van Heerden ◽  
F. J. Service ◽  
Clive S. Grant
Keyword(s):  
Surgical Management ◽  
Multiple Endocrine Neoplasia ◽  
Multiple Endocrine Neoplasia Type ◽  
Type I ◽  
Endocrine Neoplasia ◽  
Endocrine Neoplasia Type
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