Recurrent Pheochromocytoma Associated with Glucagonoma. A Case Report

Hiroshi Yao, Koshiro Fukiyama, Yuhei Kawano, Teruo Omae, Kazuhiro Mizumoto, Satoshi Toyoshima

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

We treated a hypertensive patient with recurrent pheochromocytoma (paraganglioma) associated with glucagonoma. No clinical symptom of glucagonoma was found and it could be detected only by a slight elevation of plasma immunoreactive glucagon (IRG) while the extirpated pancreatic tumor contained much IRG. This case could not be classified as either multiple endocrine neoplasia (MEN) type I or type II.

Original languageEnglish
Pages (from-to)163-166
Number of pages4
JournalEndocrinologia Japonica
Volume30
Issue number2
DOIs
Publication statusPublished - Jan 1983
Externally publishedYes

Fingerprint

Glucagonoma
Pheochromocytoma
Glucagon
Tumors
Multiple Endocrine Neoplasia Type 1
Plasmas
Paraganglioma
Neoplasms

All Science Journal Classification (ASJC) codes

  • Endocrinology
  • Engineering(all)

Cite this

Recurrent Pheochromocytoma Associated with Glucagonoma. A Case Report. / Yao, Hiroshi; Fukiyama, Koshiro; Kawano, Yuhei; Omae, Teruo; Mizumoto, Kazuhiro; Toyoshima, Satoshi.

In: Endocrinologia Japonica, Vol. 30, No. 2, 01.1983, p. 163-166.

Research output: Contribution to journalArticle

Yao, Hiroshi ; Fukiyama, Koshiro ; Kawano, Yuhei ; Omae, Teruo ; Mizumoto, Kazuhiro ; Toyoshima, Satoshi. / Recurrent Pheochromocytoma Associated with Glucagonoma. A Case Report. In: Endocrinologia Japonica. 1983 ; Vol. 30, No. 2. pp. 163-166.
@article{58302a387615460398bc6157e10a8044,
title = "Recurrent Pheochromocytoma Associated with Glucagonoma. A Case Report",
abstract = "We treated a hypertensive patient with recurrent pheochromocytoma (paraganglioma) associated with glucagonoma. No clinical symptom of glucagonoma was found and it could be detected only by a slight elevation of plasma immunoreactive glucagon (IRG) while the extirpated pancreatic tumor contained much IRG. This case could not be classified as either multiple endocrine neoplasia (MEN) type I or type II.",
author = "Hiroshi Yao and Koshiro Fukiyama and Yuhei Kawano and Teruo Omae and Kazuhiro Mizumoto and Satoshi Toyoshima",
year = "1983",
month = "1",
doi = "10.1507/endocrj1954.30.163",
language = "English",
volume = "30",
pages = "163--166",
journal = "Endocrine Journal",
issn = "0918-8959",
publisher = "Japan Endocrine Society",
number = "2",

}

TY - JOUR

T1 - Recurrent Pheochromocytoma Associated with Glucagonoma. A Case Report

AU - Yao, Hiroshi

AU - Fukiyama, Koshiro

AU - Kawano, Yuhei

AU - Omae, Teruo

AU - Mizumoto, Kazuhiro

AU - Toyoshima, Satoshi

PY - 1983/1

Y1 - 1983/1

N2 - We treated a hypertensive patient with recurrent pheochromocytoma (paraganglioma) associated with glucagonoma. No clinical symptom of glucagonoma was found and it could be detected only by a slight elevation of plasma immunoreactive glucagon (IRG) while the extirpated pancreatic tumor contained much IRG. This case could not be classified as either multiple endocrine neoplasia (MEN) type I or type II.

AB - We treated a hypertensive patient with recurrent pheochromocytoma (paraganglioma) associated with glucagonoma. No clinical symptom of glucagonoma was found and it could be detected only by a slight elevation of plasma immunoreactive glucagon (IRG) while the extirpated pancreatic tumor contained much IRG. This case could not be classified as either multiple endocrine neoplasia (MEN) type I or type II.

UR - http://www.scopus.com/inward/record.url?scp=0020617064&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0020617064&partnerID=8YFLogxK

U2 - 10.1507/endocrj1954.30.163

DO - 10.1507/endocrj1954.30.163

M3 - Article

C2 - 6139277

AN - SCOPUS:0020617064

VL - 30

SP - 163

EP - 166

JO - Endocrine Journal

JF - Endocrine Journal

SN - 0918-8959

IS - 2

ER -