Spontaneous Involution of a Presumably Rathke’s Cleft Cyst in a Patient with Slight Subclinical Hypopituitarism: A Case Report and Review of the Literature

Rathke cleft cyst is described as benign intrasellar cyst. They are mostly small and asymptomatic; they may become large enough to cause symptoms by compression of intrasellar or suprasellar structures. We report on a case of spontaneous regression of a symptomatic RCC with subsequent recovery of pr...

Full description

Saved in:
Bibliographic Details
Main Authors: Diaa Al Safatli, Rolf Kalff, Albrecht Waschke
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Case Reports in Surgery
Online Access:http://dx.doi.org/10.1155/2015/971364
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832550288576217088
author Diaa Al Safatli
Rolf Kalff
Albrecht Waschke
author_facet Diaa Al Safatli
Rolf Kalff
Albrecht Waschke
author_sort Diaa Al Safatli
collection DOAJ
description Rathke cleft cyst is described as benign intrasellar cyst. They are mostly small and asymptomatic; they may become large enough to cause symptoms by compression of intrasellar or suprasellar structures. We report on a case of spontaneous regression of a symptomatic RCC with subsequent recovery of preexisting endocrine dysfunction and resolution of headaches. A 60-year-old man complained about headaches. Laboratory investigation revealed a partial hypopituitarism with a slight central hypothyroidism without need for substitution. An MRI study showed a cystic, T2-hyperintense, sellar lesion compatible with a RCC. At one year follow-up, the patient had no complaints and the hormone work-up revealed a regression of the previous slight hypopituitarism. The MRI study showed a complete regression of the cystic lesion and a normal sized and shaped pituitary gland. The spontaneous regression of cystic sellar lesions is rare. The exact mechanism of the possible spontaneous involution of RCC is until now not well understood. However, spontaneous regression is possible and justifies the conservative therapy with regular clinical and radiological follow-up for asymptomatic patients or patients with symptoms not caused by the mass effect of these lesions.
format Article
id doaj-art-86b36eb9c5e24e0ead6f23eddbd2d654
institution Kabale University
issn 2090-6900
2090-6919
language English
publishDate 2015-01-01
publisher Wiley
record_format Article
series Case Reports in Surgery
spelling doaj-art-86b36eb9c5e24e0ead6f23eddbd2d6542025-02-03T06:07:10ZengWileyCase Reports in Surgery2090-69002090-69192015-01-01201510.1155/2015/971364971364Spontaneous Involution of a Presumably Rathke’s Cleft Cyst in a Patient with Slight Subclinical Hypopituitarism: A Case Report and Review of the LiteratureDiaa Al Safatli0Rolf Kalff1Albrecht Waschke2Department of Neurosurgery, Friedrich-Schiller University of Jena, Erlanger Allee 101, 07747 Jena, GermanyDepartment of Neurosurgery, Friedrich-Schiller University of Jena, Erlanger Allee 101, 07747 Jena, GermanyDepartment of Neurosurgery, Friedrich-Schiller University of Jena, Erlanger Allee 101, 07747 Jena, GermanyRathke cleft cyst is described as benign intrasellar cyst. They are mostly small and asymptomatic; they may become large enough to cause symptoms by compression of intrasellar or suprasellar structures. We report on a case of spontaneous regression of a symptomatic RCC with subsequent recovery of preexisting endocrine dysfunction and resolution of headaches. A 60-year-old man complained about headaches. Laboratory investigation revealed a partial hypopituitarism with a slight central hypothyroidism without need for substitution. An MRI study showed a cystic, T2-hyperintense, sellar lesion compatible with a RCC. At one year follow-up, the patient had no complaints and the hormone work-up revealed a regression of the previous slight hypopituitarism. The MRI study showed a complete regression of the cystic lesion and a normal sized and shaped pituitary gland. The spontaneous regression of cystic sellar lesions is rare. The exact mechanism of the possible spontaneous involution of RCC is until now not well understood. However, spontaneous regression is possible and justifies the conservative therapy with regular clinical and radiological follow-up for asymptomatic patients or patients with symptoms not caused by the mass effect of these lesions.http://dx.doi.org/10.1155/2015/971364
spellingShingle Diaa Al Safatli
Rolf Kalff
Albrecht Waschke
Spontaneous Involution of a Presumably Rathke’s Cleft Cyst in a Patient with Slight Subclinical Hypopituitarism: A Case Report and Review of the Literature
Case Reports in Surgery
title Spontaneous Involution of a Presumably Rathke’s Cleft Cyst in a Patient with Slight Subclinical Hypopituitarism: A Case Report and Review of the Literature
title_full Spontaneous Involution of a Presumably Rathke’s Cleft Cyst in a Patient with Slight Subclinical Hypopituitarism: A Case Report and Review of the Literature
title_fullStr Spontaneous Involution of a Presumably Rathke’s Cleft Cyst in a Patient with Slight Subclinical Hypopituitarism: A Case Report and Review of the Literature
title_full_unstemmed Spontaneous Involution of a Presumably Rathke’s Cleft Cyst in a Patient with Slight Subclinical Hypopituitarism: A Case Report and Review of the Literature
title_short Spontaneous Involution of a Presumably Rathke’s Cleft Cyst in a Patient with Slight Subclinical Hypopituitarism: A Case Report and Review of the Literature
title_sort spontaneous involution of a presumably rathke s cleft cyst in a patient with slight subclinical hypopituitarism a case report and review of the literature
url http://dx.doi.org/10.1155/2015/971364
work_keys_str_mv AT diaaalsafatli spontaneousinvolutionofapresumablyrathkescleftcystinapatientwithslightsubclinicalhypopituitarismacasereportandreviewoftheliterature
AT rolfkalff spontaneousinvolutionofapresumablyrathkescleftcystinapatientwithslightsubclinicalhypopituitarismacasereportandreviewoftheliterature
AT albrechtwaschke spontaneousinvolutionofapresumablyrathkescleftcystinapatientwithslightsubclinicalhypopituitarismacasereportandreviewoftheliterature