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Symptomatic hypopituitarism revealing primary suprasellar lymphoma
BACKGROUND: The most common cause of hypopituitarism is pituitary adenoma. However, in the case of suprasellar masses different etiologies are possible. We report an unusual case of primary suprasellar lymphoma presented with hypopituitarism. CASE PRESENTATION: A 26 year old woman presented with ame...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006376/ https://www.ncbi.nlm.nih.gov/pubmed/21114849 http://dx.doi.org/10.1186/1472-6823-10-19 |
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author | Fadoukhair, Zouhour Amzerin, Mounia Ismaili, Nabil Belbaraka, Rhizlane Latib, Rachida Sbitti, Yassir M'rabti, Hind Boutayeb, Saber Ichou, Mohammed Errihani, Hassan |
author_facet | Fadoukhair, Zouhour Amzerin, Mounia Ismaili, Nabil Belbaraka, Rhizlane Latib, Rachida Sbitti, Yassir M'rabti, Hind Boutayeb, Saber Ichou, Mohammed Errihani, Hassan |
author_sort | Fadoukhair, Zouhour |
collection | PubMed |
description | BACKGROUND: The most common cause of hypopituitarism is pituitary adenoma. However, in the case of suprasellar masses different etiologies are possible. We report an unusual case of primary suprasellar lymphoma presented with hypopituitarism. CASE PRESENTATION: A 26 year old woman presented with amenorrhea, galactorrhea and neurological disorders. Also, the laboratory work-up revealed partial hypopituitarism. The magnetic resonance imaging of the head showed a suprasellar mass. A presumptive diagnosis of granulomatous processes was made and the patient was given steroid therapy. Repeated brain MRI detected new lesions in the brain with regression of the suprasellar mass. Stereotactic biopsy of the paraventricular lesion revealed the diagnosis of B-cell lymphoma. CONCLUSION: This case presentation reports a rare cause of hypopituitarism. Primary suprasellar lymphoma is extremely rare and represented a real diagnostic challenge. Besides, suprasellar masses are varied in aetiology and can present diagnostic problems for a radiologist. Also, because of the increased incidence of PCNSL, lymphoma must be kept in mind in the differential diagnosis of lesions in the suprasellar region. |
format | Text |
id | pubmed-3006376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30063762010-12-22 Symptomatic hypopituitarism revealing primary suprasellar lymphoma Fadoukhair, Zouhour Amzerin, Mounia Ismaili, Nabil Belbaraka, Rhizlane Latib, Rachida Sbitti, Yassir M'rabti, Hind Boutayeb, Saber Ichou, Mohammed Errihani, Hassan BMC Endocr Disord Case Report BACKGROUND: The most common cause of hypopituitarism is pituitary adenoma. However, in the case of suprasellar masses different etiologies are possible. We report an unusual case of primary suprasellar lymphoma presented with hypopituitarism. CASE PRESENTATION: A 26 year old woman presented with amenorrhea, galactorrhea and neurological disorders. Also, the laboratory work-up revealed partial hypopituitarism. The magnetic resonance imaging of the head showed a suprasellar mass. A presumptive diagnosis of granulomatous processes was made and the patient was given steroid therapy. Repeated brain MRI detected new lesions in the brain with regression of the suprasellar mass. Stereotactic biopsy of the paraventricular lesion revealed the diagnosis of B-cell lymphoma. CONCLUSION: This case presentation reports a rare cause of hypopituitarism. Primary suprasellar lymphoma is extremely rare and represented a real diagnostic challenge. Besides, suprasellar masses are varied in aetiology and can present diagnostic problems for a radiologist. Also, because of the increased incidence of PCNSL, lymphoma must be kept in mind in the differential diagnosis of lesions in the suprasellar region. BioMed Central 2010-11-29 /pmc/articles/PMC3006376/ /pubmed/21114849 http://dx.doi.org/10.1186/1472-6823-10-19 Text en Copyright ©2010 Fadoukhair et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Fadoukhair, Zouhour Amzerin, Mounia Ismaili, Nabil Belbaraka, Rhizlane Latib, Rachida Sbitti, Yassir M'rabti, Hind Boutayeb, Saber Ichou, Mohammed Errihani, Hassan Symptomatic hypopituitarism revealing primary suprasellar lymphoma |
title | Symptomatic hypopituitarism revealing primary suprasellar lymphoma |
title_full | Symptomatic hypopituitarism revealing primary suprasellar lymphoma |
title_fullStr | Symptomatic hypopituitarism revealing primary suprasellar lymphoma |
title_full_unstemmed | Symptomatic hypopituitarism revealing primary suprasellar lymphoma |
title_short | Symptomatic hypopituitarism revealing primary suprasellar lymphoma |
title_sort | symptomatic hypopituitarism revealing primary suprasellar lymphoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006376/ https://www.ncbi.nlm.nih.gov/pubmed/21114849 http://dx.doi.org/10.1186/1472-6823-10-19 |
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