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Clival ectopic pituitary prolactinoma was successfully managed by transsphenoidal surgery: A rare case report

KEY CLINICAL MESSAGE: Ectopic pituitary adenoma is a rare neoplasm located in the clivus and could mimic other clival tumors. Diagnosis and treatment could be challenging. It should be considered in the differential diagnosis of clival tumors. ABSTRACT: Ectopic pituitary adenomas (EPAs) are isolated...

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Autores principales: Mansour, Marah, Khozamah, Zeinah, Naksho, Abdulmonem, Zayat, Roaa, Al Sabbagh, Aliaa, Deeb, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661317/
https://www.ncbi.nlm.nih.gov/pubmed/38028100
http://dx.doi.org/10.1002/ccr3.8255
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author Mansour, Marah
Khozamah, Zeinah
Naksho, Abdulmonem
Zayat, Roaa
Al Sabbagh, Aliaa
Deeb, Ahmad
author_facet Mansour, Marah
Khozamah, Zeinah
Naksho, Abdulmonem
Zayat, Roaa
Al Sabbagh, Aliaa
Deeb, Ahmad
author_sort Mansour, Marah
collection PubMed
description KEY CLINICAL MESSAGE: Ectopic pituitary adenoma is a rare neoplasm located in the clivus and could mimic other clival tumors. Diagnosis and treatment could be challenging. It should be considered in the differential diagnosis of clival tumors. ABSTRACT: Ectopic pituitary adenomas (EPAs) are isolated adenomas that can be located in variable locations outside the sella turcica and have a normal‐appearing pituitary gland. These tumors are rare and are thought to often arise from embryological remnants along the route of Rathke's pouch migration. EPAs are associated with a wide range of clinical manifestations depending on hormonal activity and involvement of adjacent structures, which can represent a challenge in making the diagnosis and deciding on the most appropriate management. In this case study, we report a 47‐year‐old male who presented with visual disturbances, a headache, and generalized weakness. Magnetic resonance imaging showed a 2 cm mass located in the clivus invading the sphenoid sinus with an intact pituitary gland. The patient underwent endoscopic transsphenoidal surgery to eradicate the mass while maintaining the integrity of the pituitary gland, which was successful and uneventful. Pathological studies were consistent with prolactinoma, with no cytological malignant features. Post‐surgery, symptoms notably improved, and serum prolactin levels significantly dropped, The patient's condition was satisfactory on follow‐up with no long‐term complications reported. This paper contributes to the existing literature by sharing the clinical management of a challenging and uncommon case.
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spelling pubmed-106613172023-11-20 Clival ectopic pituitary prolactinoma was successfully managed by transsphenoidal surgery: A rare case report Mansour, Marah Khozamah, Zeinah Naksho, Abdulmonem Zayat, Roaa Al Sabbagh, Aliaa Deeb, Ahmad Clin Case Rep Case Report KEY CLINICAL MESSAGE: Ectopic pituitary adenoma is a rare neoplasm located in the clivus and could mimic other clival tumors. Diagnosis and treatment could be challenging. It should be considered in the differential diagnosis of clival tumors. ABSTRACT: Ectopic pituitary adenomas (EPAs) are isolated adenomas that can be located in variable locations outside the sella turcica and have a normal‐appearing pituitary gland. These tumors are rare and are thought to often arise from embryological remnants along the route of Rathke's pouch migration. EPAs are associated with a wide range of clinical manifestations depending on hormonal activity and involvement of adjacent structures, which can represent a challenge in making the diagnosis and deciding on the most appropriate management. In this case study, we report a 47‐year‐old male who presented with visual disturbances, a headache, and generalized weakness. Magnetic resonance imaging showed a 2 cm mass located in the clivus invading the sphenoid sinus with an intact pituitary gland. The patient underwent endoscopic transsphenoidal surgery to eradicate the mass while maintaining the integrity of the pituitary gland, which was successful and uneventful. Pathological studies were consistent with prolactinoma, with no cytological malignant features. Post‐surgery, symptoms notably improved, and serum prolactin levels significantly dropped, The patient's condition was satisfactory on follow‐up with no long‐term complications reported. This paper contributes to the existing literature by sharing the clinical management of a challenging and uncommon case. John Wiley and Sons Inc. 2023-11-20 /pmc/articles/PMC10661317/ /pubmed/38028100 http://dx.doi.org/10.1002/ccr3.8255 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mansour, Marah
Khozamah, Zeinah
Naksho, Abdulmonem
Zayat, Roaa
Al Sabbagh, Aliaa
Deeb, Ahmad
Clival ectopic pituitary prolactinoma was successfully managed by transsphenoidal surgery: A rare case report
title Clival ectopic pituitary prolactinoma was successfully managed by transsphenoidal surgery: A rare case report
title_full Clival ectopic pituitary prolactinoma was successfully managed by transsphenoidal surgery: A rare case report
title_fullStr Clival ectopic pituitary prolactinoma was successfully managed by transsphenoidal surgery: A rare case report
title_full_unstemmed Clival ectopic pituitary prolactinoma was successfully managed by transsphenoidal surgery: A rare case report
title_short Clival ectopic pituitary prolactinoma was successfully managed by transsphenoidal surgery: A rare case report
title_sort clival ectopic pituitary prolactinoma was successfully managed by transsphenoidal surgery: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661317/
https://www.ncbi.nlm.nih.gov/pubmed/38028100
http://dx.doi.org/10.1002/ccr3.8255
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