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Pheochromocytoma presenting as recurrent urinary tract infections : a case report
INTRODUCTION: Pheochromocytomas are rare, potentially fatal, neuroendocrine tumors of the adrenal medulla or extra-adrenal paraganglia. Their clinical presentation varies greatly from the classic triad of episodic headache, diaphoresis and tachycardia to include a spectrum of non-specific symptomato...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025966/ https://www.ncbi.nlm.nih.gov/pubmed/21226896 http://dx.doi.org/10.1186/1752-1947-5-6 |
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author | Dolan, Roisin T Butler, Joseph S McEntee, Gerard P Byrne, Maria M |
author_facet | Dolan, Roisin T Butler, Joseph S McEntee, Gerard P Byrne, Maria M |
author_sort | Dolan, Roisin T |
collection | PubMed |
description | INTRODUCTION: Pheochromocytomas are rare, potentially fatal, neuroendocrine tumors of the adrenal medulla or extra-adrenal paraganglia. Their clinical presentation varies greatly from the classic triad of episodic headache, diaphoresis and tachycardia to include a spectrum of non-specific symptomatology. CASE PRESENTATION: A 43-year-old Caucasian woman was referred to us from primary care services with a three-month history of recurrent urinary tract infections on a background of hypertension, latent autoimmune diabetes of adulthood and autoimmune hypothyroidism. At 38 years she required insulin therapy. Despite medication compliance and dietary control, she reported a recent history of increased insulin requirements and uncontrolled hypertension with concomitant recurrent urinary tract infections. A renal ultrasound examination, to rule out underlying renal pathology, revealed an incidental 8cm right adrenal mass of both solid and cystic components. A subsequent computed tomography of her abdomen and pelvis confirmed a solid heterogeneous mass consistent with a pheochromocytoma. There were no other features suggestive of multiple endocrine neoplasia. Urinary collection over 24 hours revealed grossly elevated levels of catecholamines and metabolites. Following an open right adrenalectomy, our patient's insulin requirements were significantly reduced and her symptoms resolved. Two weeks post-operatively, an iodine-131-metaiodobenzylguanidine scintigraphy was negative for residual tumor and metastatic disease. Urinary catecholamine and metabolite concentrations were within the normal range at a follow-up six months later. CONCLUSION: Pheochromocytoma is a rare catecholamine-producing tumor requiring a high index of suspicion for early diagnosis. Our case report serves to highlight the importance of considering pheochromocytoma as a differential diagnosis in the atypical setting of recurrent urinary tract infections and concomitant autoimmune disease. |
format | Text |
id | pubmed-3025966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30259662011-01-25 Pheochromocytoma presenting as recurrent urinary tract infections : a case report Dolan, Roisin T Butler, Joseph S McEntee, Gerard P Byrne, Maria M J Med Case Reports Case Report INTRODUCTION: Pheochromocytomas are rare, potentially fatal, neuroendocrine tumors of the adrenal medulla or extra-adrenal paraganglia. Their clinical presentation varies greatly from the classic triad of episodic headache, diaphoresis and tachycardia to include a spectrum of non-specific symptomatology. CASE PRESENTATION: A 43-year-old Caucasian woman was referred to us from primary care services with a three-month history of recurrent urinary tract infections on a background of hypertension, latent autoimmune diabetes of adulthood and autoimmune hypothyroidism. At 38 years she required insulin therapy. Despite medication compliance and dietary control, she reported a recent history of increased insulin requirements and uncontrolled hypertension with concomitant recurrent urinary tract infections. A renal ultrasound examination, to rule out underlying renal pathology, revealed an incidental 8cm right adrenal mass of both solid and cystic components. A subsequent computed tomography of her abdomen and pelvis confirmed a solid heterogeneous mass consistent with a pheochromocytoma. There were no other features suggestive of multiple endocrine neoplasia. Urinary collection over 24 hours revealed grossly elevated levels of catecholamines and metabolites. Following an open right adrenalectomy, our patient's insulin requirements were significantly reduced and her symptoms resolved. Two weeks post-operatively, an iodine-131-metaiodobenzylguanidine scintigraphy was negative for residual tumor and metastatic disease. Urinary catecholamine and metabolite concentrations were within the normal range at a follow-up six months later. CONCLUSION: Pheochromocytoma is a rare catecholamine-producing tumor requiring a high index of suspicion for early diagnosis. Our case report serves to highlight the importance of considering pheochromocytoma as a differential diagnosis in the atypical setting of recurrent urinary tract infections and concomitant autoimmune disease. BioMed Central 2011-01-12 /pmc/articles/PMC3025966/ /pubmed/21226896 http://dx.doi.org/10.1186/1752-1947-5-6 Text en Copyright ©2011 Dolan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Dolan, Roisin T Butler, Joseph S McEntee, Gerard P Byrne, Maria M Pheochromocytoma presenting as recurrent urinary tract infections : a case report |
title | Pheochromocytoma presenting as recurrent urinary tract infections : a case report |
title_full | Pheochromocytoma presenting as recurrent urinary tract infections : a case report |
title_fullStr | Pheochromocytoma presenting as recurrent urinary tract infections : a case report |
title_full_unstemmed | Pheochromocytoma presenting as recurrent urinary tract infections : a case report |
title_short | Pheochromocytoma presenting as recurrent urinary tract infections : a case report |
title_sort | pheochromocytoma presenting as recurrent urinary tract infections : a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025966/ https://www.ncbi.nlm.nih.gov/pubmed/21226896 http://dx.doi.org/10.1186/1752-1947-5-6 |
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