Early surgical intervention for patients with possible clinically silent somatotroph adenoma: a case series

Abstract Introduction Clinically silent somatotroph adenoma is characterized by elevated serum growth hormone but without the clinical symptoms of acromegaly, and it is considered rare. The natural history is not well understood, progress to symptomatic is uncertain, and treatment strategy has not b...

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Main Authors: Tomohiro Kawaguchi, Yoshikazu Ogawa, Teiji Tominaga
Format: Article
Language:English
Published: BMC 2019-03-01
Series:Journal of Medical Case Reports
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13256-019-1981-3
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spelling doaj-6a07392aa25a4dfca2dc8285132ff7232020-11-25T03:19:31ZengBMCJournal of Medical Case Reports1752-19472019-03-011311610.1186/s13256-019-1981-3Early surgical intervention for patients with possible clinically silent somatotroph adenoma: a case seriesTomohiro Kawaguchi0Yoshikazu Ogawa1Teiji Tominaga2Department of Neurosurgery, Tohoku University Graduate School of MedicineDepartment of Neurosurgery, Kohnan HospitalDepartment of Neurosurgery, Tohoku University Graduate School of MedicineAbstract Introduction Clinically silent somatotroph adenoma is characterized by elevated serum growth hormone but without the clinical symptoms of acromegaly, and it is considered rare. The natural history is not well understood, progress to symptomatic is uncertain, and treatment strategy has not been established. Case presentation The first patient was a 48-year-old-Asian woman who presented with serum growth hormone 6.99 ng/ml and insulin-like growth factor 1 of 476 ng/ml, but no characteristic features of acromegaly. Five years after initial diagnosis, she presented with acromegalic facial appearance. Transsphenoidal surgery achieved gross total removal and endocrinological remission. The second patient was a 40-year-old-Asian woman who presented with serum growth hormone 31.14 ng/ml and insulin-like growth factor 1 of 709.6 ng/ml, but no characteristic features of acromegaly. Three years after initial diagnosis, she presented with acromegalic facial appearance. Transsphenoidal surgery achieved gross total removal and endocrinological remission. The third patient was a 64-year-old-Asian woman who presented with serum growth hormone 6.0 ng/ml and insulin-like growth factor 1 of 341 ng/ml, but no characteristic features of acromegaly. Eight months after initial diagnosis, hand enlargement was detected. Transsphenoidal surgery achieved gross total removal and endocrinological remission. Conclusion Due to its potential for evolving to symptomatic disease, the risks of surgery and observation for patients with somatotroph adenoma should be carefully compared from the viewpoint of better health outcome.http://link.springer.com/article/10.1186/s13256-019-1981-3AcromegalyClinically silentGrowth hormoneSomatotroph adenomaTranssphenoidal surgery
collection DOAJ
language English
format Article
sources DOAJ
author Tomohiro Kawaguchi
Yoshikazu Ogawa
Teiji Tominaga
spellingShingle Tomohiro Kawaguchi
Yoshikazu Ogawa
Teiji Tominaga
Early surgical intervention for patients with possible clinically silent somatotroph adenoma: a case series
Journal of Medical Case Reports
Acromegaly
Clinically silent
Growth hormone
Somatotroph adenoma
Transsphenoidal surgery
author_facet Tomohiro Kawaguchi
Yoshikazu Ogawa
Teiji Tominaga
author_sort Tomohiro Kawaguchi
title Early surgical intervention for patients with possible clinically silent somatotroph adenoma: a case series
title_short Early surgical intervention for patients with possible clinically silent somatotroph adenoma: a case series
title_full Early surgical intervention for patients with possible clinically silent somatotroph adenoma: a case series
title_fullStr Early surgical intervention for patients with possible clinically silent somatotroph adenoma: a case series
title_full_unstemmed Early surgical intervention for patients with possible clinically silent somatotroph adenoma: a case series
title_sort early surgical intervention for patients with possible clinically silent somatotroph adenoma: a case series
publisher BMC
series Journal of Medical Case Reports
issn 1752-1947
publishDate 2019-03-01
description Abstract Introduction Clinically silent somatotroph adenoma is characterized by elevated serum growth hormone but without the clinical symptoms of acromegaly, and it is considered rare. The natural history is not well understood, progress to symptomatic is uncertain, and treatment strategy has not been established. Case presentation The first patient was a 48-year-old-Asian woman who presented with serum growth hormone 6.99 ng/ml and insulin-like growth factor 1 of 476 ng/ml, but no characteristic features of acromegaly. Five years after initial diagnosis, she presented with acromegalic facial appearance. Transsphenoidal surgery achieved gross total removal and endocrinological remission. The second patient was a 40-year-old-Asian woman who presented with serum growth hormone 31.14 ng/ml and insulin-like growth factor 1 of 709.6 ng/ml, but no characteristic features of acromegaly. Three years after initial diagnosis, she presented with acromegalic facial appearance. Transsphenoidal surgery achieved gross total removal and endocrinological remission. The third patient was a 64-year-old-Asian woman who presented with serum growth hormone 6.0 ng/ml and insulin-like growth factor 1 of 341 ng/ml, but no characteristic features of acromegaly. Eight months after initial diagnosis, hand enlargement was detected. Transsphenoidal surgery achieved gross total removal and endocrinological remission. Conclusion Due to its potential for evolving to symptomatic disease, the risks of surgery and observation for patients with somatotroph adenoma should be carefully compared from the viewpoint of better health outcome.
topic Acromegaly
Clinically silent
Growth hormone
Somatotroph adenoma
Transsphenoidal surgery
url http://link.springer.com/article/10.1186/s13256-019-1981-3
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