Erdheim‐Chester disease with long‐standing diabetes insipidus and generalized edema

Abstract Erdheim‐Chester disease (ECD) is a rare non‐Langerhans histiocytosis. ECD is detected more frequently due to increased awareness of healthcare providers and improved diagnostic tools. This report describes a 51‐year‐old woman with a history of weakness, bone pain, xanthelasma palpebrarum, a...

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Autores principales:	Faezeh Sadat Naji, Minoo Sadat Hajmiri, Zahra Mazari, Faeze Salahshour, Vahid Soleimani, Manouchehr Nakhjavani, Mahboobeh Hemmatabadi
Formato:	article
Lenguaje:	EN
Publicado:	Wiley 2021
Materias:	diabetes insipidus Erdheim‐Chester disease non‐langerhans‐cell histiocytosis Medicine R Medicine (General) R5-920
Acceso en línea:	https://doaj.org/article/be4e4e7226b849178673b102528f7d87
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spelling	oai:doaj.org-article:be4e4e7226b849178673b102528f7d872021-12-02T07:55:56ZErdheim‐Chester disease with long‐standing diabetes insipidus and generalized edema2050-090410.1002/ccr3.4898https://doaj.org/article/be4e4e7226b849178673b102528f7d872021-10-01T00:00:00Zhttps://doi.org/10.1002/ccr3.4898https://doaj.org/toc/2050-0904Abstract Erdheim‐Chester disease (ECD) is a rare non‐Langerhans histiocytosis. ECD is detected more frequently due to increased awareness of healthcare providers and improved diagnostic tools. This report describes a 51‐year‐old woman with a history of weakness, bone pain, xanthelasma palpebrarum, and diabetes insipidus. ECD is a multisystemic condition with a poor prognosis. This disease should be considered in patients with diabetes insipidus, bone pain, and multiorgan involvements.Faezeh Sadat NajiMinoo Sadat HajmiriZahra MazariFaeze SalahshourVahid SoleimaniManouchehr NakhjavaniMahboobeh HemmatabadiWileyarticlediabetes insipidusErdheim‐Chester diseasenon‐langerhans‐cell histiocytosisMedicineRMedicine (General)R5-920ENClinical Case Reports, Vol 9, Iss 10, Pp n/a-n/a (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	diabetes insipidus Erdheim‐Chester disease non‐langerhans‐cell histiocytosis Medicine R Medicine (General) R5-920
spellingShingle	diabetes insipidus Erdheim‐Chester disease non‐langerhans‐cell histiocytosis Medicine R Medicine (General) R5-920 Faezeh Sadat Naji Minoo Sadat Hajmiri Zahra Mazari Faeze Salahshour Vahid Soleimani Manouchehr Nakhjavani Mahboobeh Hemmatabadi Erdheim‐Chester disease with long‐standing diabetes insipidus and generalized edema
description	Abstract Erdheim‐Chester disease (ECD) is a rare non‐Langerhans histiocytosis. ECD is detected more frequently due to increased awareness of healthcare providers and improved diagnostic tools. This report describes a 51‐year‐old woman with a history of weakness, bone pain, xanthelasma palpebrarum, and diabetes insipidus. ECD is a multisystemic condition with a poor prognosis. This disease should be considered in patients with diabetes insipidus, bone pain, and multiorgan involvements.
format	article
author	Faezeh Sadat Naji Minoo Sadat Hajmiri Zahra Mazari Faeze Salahshour Vahid Soleimani Manouchehr Nakhjavani Mahboobeh Hemmatabadi
author_facet	Faezeh Sadat Naji Minoo Sadat Hajmiri Zahra Mazari Faeze Salahshour Vahid Soleimani Manouchehr Nakhjavani Mahboobeh Hemmatabadi
author_sort	Faezeh Sadat Naji
title	Erdheim‐Chester disease with long‐standing diabetes insipidus and generalized edema
title_short	Erdheim‐Chester disease with long‐standing diabetes insipidus and generalized edema
title_full	Erdheim‐Chester disease with long‐standing diabetes insipidus and generalized edema
title_fullStr	Erdheim‐Chester disease with long‐standing diabetes insipidus and generalized edema
title_full_unstemmed	Erdheim‐Chester disease with long‐standing diabetes insipidus and generalized edema
title_sort	erdheim‐chester disease with long‐standing diabetes insipidus and generalized edema
publisher	Wiley
publishDate	2021
url	https://doaj.org/article/be4e4e7226b849178673b102528f7d87
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Erdheim‐Chester disease with long‐standing diabetes insipidus and generalized edema

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