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MON-381 A Missed Case of Pheochromocytoma in NF1 Patient Presenting as Pre-Eclampsia
Background Neurofibromatosis type 1 (NF1) is a rare autosomal dominant disorder manifesting with skin lesions and neurofibromas. An increased risk of pheochromocytoma and paraganglioma (PPGL) is known with an estimated incidence of 0.1-5.7%(1). While some data suggested screening for PPGL in NF1 pat...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Endocrine Society
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550592/ http://dx.doi.org/10.1210/js.2019-MON-381 |