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Primary pigmented nodular adrenocortical disease
Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of ACTH-independent Cushing's syndrome and has characteristic gross and microscopic pathologic findings. We report a case of PPNAD in a 15-year-old boy, which was not associated with Carney's complex. Bilateral adrena...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221162/ https://www.ncbi.nlm.nih.gov/pubmed/22121318 http://dx.doi.org/10.4103/0971-9261.86881 |
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author | Manipadam, Marie T. Abraham, Rachel Sen, Sudipta Simon, Anna |
author_facet | Manipadam, Marie T. Abraham, Rachel Sen, Sudipta Simon, Anna |
author_sort | Manipadam, Marie T. |
collection | PubMed |
description | Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of ACTH-independent Cushing's syndrome and has characteristic gross and microscopic pathologic findings. We report a case of PPNAD in a 15-year-old boy, which was not associated with Carney's complex. Bilateral adrenalectomy is the treatment of choice. |
format | Online Article Text |
id | pubmed-3221162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32211622011-11-25 Primary pigmented nodular adrenocortical disease Manipadam, Marie T. Abraham, Rachel Sen, Sudipta Simon, Anna J Indian Assoc Pediatr Surg Case Report Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of ACTH-independent Cushing's syndrome and has characteristic gross and microscopic pathologic findings. We report a case of PPNAD in a 15-year-old boy, which was not associated with Carney's complex. Bilateral adrenalectomy is the treatment of choice. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3221162/ /pubmed/22121318 http://dx.doi.org/10.4103/0971-9261.86881 Text en Copyright: © Journal of Indian Association of Pediatric Surgeons http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Manipadam, Marie T. Abraham, Rachel Sen, Sudipta Simon, Anna Primary pigmented nodular adrenocortical disease |
title | Primary pigmented nodular adrenocortical disease |
title_full | Primary pigmented nodular adrenocortical disease |
title_fullStr | Primary pigmented nodular adrenocortical disease |
title_full_unstemmed | Primary pigmented nodular adrenocortical disease |
title_short | Primary pigmented nodular adrenocortical disease |
title_sort | primary pigmented nodular adrenocortical disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221162/ https://www.ncbi.nlm.nih.gov/pubmed/22121318 http://dx.doi.org/10.4103/0971-9261.86881 |
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