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Pituitary Carcinoma in a Patient with Cowden Syndrome

Patient: Female, 58-year-old Final Diagnosis: Pituitary carcinoma Symptoms: Headache • left temporal lower quadrantanopia • right temporal hemianopia Medication: — Clinical Procedure: — Specialty: Neurology • Neurosurgery • Radiology • Pathology OBJECTIVE: Rare coexistence of disease or pathology BA...

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Detalles Bibliográficos
Autores principales: Zhang, Han, Li, Junsiyuan, Lee, Ming, Ho, Chi Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822848/
https://www.ncbi.nlm.nih.gov/pubmed/35110519
http://dx.doi.org/10.12659/AJCR.934846
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author Zhang, Han
Li, Junsiyuan
Lee, Ming
Ho, Chi Long
author_facet Zhang, Han
Li, Junsiyuan
Lee, Ming
Ho, Chi Long
author_sort Zhang, Han
collection PubMed
description Patient: Female, 58-year-old Final Diagnosis: Pituitary carcinoma Symptoms: Headache • left temporal lower quadrantanopia • right temporal hemianopia Medication: — Clinical Procedure: — Specialty: Neurology • Neurosurgery • Radiology • Pathology OBJECTIVE: Rare coexistence of disease or pathology BACKGROUND: Pituitary carcinomas are rare tumors that are histologically indistinguishable from pituitary adenoma. This report describes an extremely rare case of pituitary carcinoma in a patient with clinically diagnosed Cowden syndrome (CS). CS is a rare multisystemic hereditary disease with increase risks of cancer and benign overgrowth of different types of tissues. CASE REPORT: A 52-year-old woman with history of CS presented with pituitary adenoma and multiple meningiomata. After surgical resection, there was recurrence of the pituitary tumor. Partial resection of the recurrent pituitary tumor revealed an adenoma. Radiotherapy was administered due to the histopathological aggressive features of the resected pituitary tumor and growth of the residual pituitary tumor on follow-up. Although the pituitary tumor shrank after radiotherapy, there was development of multiple new intracranial extra-axial lesions. Resection of a rapidly growing extra-axial tumor in the parietal convexity region was performed. Given the similar histo-pathological features of the convexity tumor with the prior pituitary specimen, the diagnosis of pituitary carcinoma was established. A subsequent MRI scan showed metastatic deposits along the spine. The patient’s condition deteriorated and she died shortly after the last surgery. CONCLUSIONS: To the best of our knowledge, there is no prior report of pituitary carcinoma in a patient with CS in the literature. Pituitary carcinomas frequently spread within the craniospinal axis, in addition to hematogenous dissemination. Given the high risks of developing malignant tumors in patients with CS, multidisciplinary management including diagnostic imaging and close surveillance are of paramount importance in patient management.
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spelling pubmed-88228482022-02-24 Pituitary Carcinoma in a Patient with Cowden Syndrome Zhang, Han Li, Junsiyuan Lee, Ming Ho, Chi Long Am J Case Rep Articles Patient: Female, 58-year-old Final Diagnosis: Pituitary carcinoma Symptoms: Headache • left temporal lower quadrantanopia • right temporal hemianopia Medication: — Clinical Procedure: — Specialty: Neurology • Neurosurgery • Radiology • Pathology OBJECTIVE: Rare coexistence of disease or pathology BACKGROUND: Pituitary carcinomas are rare tumors that are histologically indistinguishable from pituitary adenoma. This report describes an extremely rare case of pituitary carcinoma in a patient with clinically diagnosed Cowden syndrome (CS). CS is a rare multisystemic hereditary disease with increase risks of cancer and benign overgrowth of different types of tissues. CASE REPORT: A 52-year-old woman with history of CS presented with pituitary adenoma and multiple meningiomata. After surgical resection, there was recurrence of the pituitary tumor. Partial resection of the recurrent pituitary tumor revealed an adenoma. Radiotherapy was administered due to the histopathological aggressive features of the resected pituitary tumor and growth of the residual pituitary tumor on follow-up. Although the pituitary tumor shrank after radiotherapy, there was development of multiple new intracranial extra-axial lesions. Resection of a rapidly growing extra-axial tumor in the parietal convexity region was performed. Given the similar histo-pathological features of the convexity tumor with the prior pituitary specimen, the diagnosis of pituitary carcinoma was established. A subsequent MRI scan showed metastatic deposits along the spine. The patient’s condition deteriorated and she died shortly after the last surgery. CONCLUSIONS: To the best of our knowledge, there is no prior report of pituitary carcinoma in a patient with CS in the literature. Pituitary carcinomas frequently spread within the craniospinal axis, in addition to hematogenous dissemination. Given the high risks of developing malignant tumors in patients with CS, multidisciplinary management including diagnostic imaging and close surveillance are of paramount importance in patient management. International Scientific Literature, Inc. 2022-02-03 /pmc/articles/PMC8822848/ /pubmed/35110519 http://dx.doi.org/10.12659/AJCR.934846 Text en © Am J Case Rep, 2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Zhang, Han
Li, Junsiyuan
Lee, Ming
Ho, Chi Long
Pituitary Carcinoma in a Patient with Cowden Syndrome
title Pituitary Carcinoma in a Patient with Cowden Syndrome
title_full Pituitary Carcinoma in a Patient with Cowden Syndrome
title_fullStr Pituitary Carcinoma in a Patient with Cowden Syndrome
title_full_unstemmed Pituitary Carcinoma in a Patient with Cowden Syndrome
title_short Pituitary Carcinoma in a Patient with Cowden Syndrome
title_sort pituitary carcinoma in a patient with cowden syndrome
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822848/
https://www.ncbi.nlm.nih.gov/pubmed/35110519
http://dx.doi.org/10.12659/AJCR.934846
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