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...
Saved in:
Main Authors: | , , |
---|---|
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 |