Clinical and Diagnostic Imaging Manifestations of Erdheim-Chester Disease

Christina E. Borchers; Roland Gazaille; Avrey Thau; Alejandro Calvo; Ronald E. Warwar; William Boyce; Joseph Blake

Clinical and Diagnostic Imaging Manifestations of Erdheim-Chester Disease

Christina E. Borchers, Roland Gazaille, Avrey Thau, Alejandro Calvo, Ronald E. Warwar, William Boyce, Joseph Blake

Dermatology

Research output: Contribution to conference › Presentation

Abstract

Erdheim-Chester Disease (ECD) is a rare form of non-Langerhans-
cell histiocytosis. Since its first description in 1930 by Jakob Erdheim
and William Chester, approximately 1500 cases have been reported
world-wide. Despite the majority of literature comprised by case
reports, a predilection for males in their 5th and 7th decade of life with
multisystem involvement that may include dermatologic systems,
central nervous system, skeletal, cardiovascular, renal systems have
been frequently reported. The presenting symptoms most commonly
include fatty nodules on the eyelids (xanthelasma) and cutaneous
xanthomas-like lesions of the skin, proptosis, diabetes insipidus,
dysarthria, headache, lower extremity bone pain and imbalance,
although many others have been described.

Original language	American English
State	Published - Sep 12 2020
Event	Inaugural 2020 San Diego Dermatology Symposium - San Diego, United States Duration: Sep 11 2020 → Sep 13 2020

Conference

Conference	Inaugural 2020 San Diego Dermatology Symposium
Country/Territory	United States
City	San Diego
Period	9/11/20 → 9/13/20

Disciplines

Medicine and Health Sciences

Access to Document

Wright State University- Borchers 2.pdfFinal published version, 14.1 MBLicense: Unspecified

Cite this

@conference{a8f9e1e147314b1db46f0a41565a3336,

title = "Clinical and Diagnostic Imaging Manifestations of Erdheim-Chester Disease",

abstract = "Erdheim-Chester Disease (ECD) is a rare form of non-Langerhans-cell histiocytosis. Since its first description in 1930 by Jakob Erdheimand William Chester, approximately 1500 cases have been reportedworld-wide. Despite the majority of literature comprised by casereports, a predilection for males in their 5th and 7th decade of life withmultisystem involvement that may include dermatologic systems,central nervous system, skeletal, cardiovascular, renal systems havebeen frequently reported. The presenting symptoms most commonlyinclude fatty nodules on the eyelids (xanthelasma) and cutaneousxanthomas-like lesions of the skin, proptosis, diabetes insipidus,dysarthria, headache, lower extremity bone pain and imbalance,although many others have been described.",

author = "Borchers, {Christina E.} and Roland Gazaille and Avrey Thau and Alejandro Calvo and Warwar, {Ronald E.} and William Boyce and Joseph Blake",

year = "2020",

month = sep,

day = "12",

language = "American English",

note = "Inaugural 2020 San Diego Dermatology Symposium ; Conference date: 11-09-2020 Through 13-09-2020",

}

TY - CONF

T1 - Clinical and Diagnostic Imaging Manifestations of Erdheim-Chester Disease

AU - Borchers, Christina E.

AU - Gazaille, Roland

AU - Thau, Avrey

AU - Calvo, Alejandro

AU - Warwar, Ronald E.

AU - Boyce, William

AU - Blake, Joseph

PY - 2020/9/12

Y1 - 2020/9/12

N2 - Erdheim-Chester Disease (ECD) is a rare form of non-Langerhans-cell histiocytosis. Since its first description in 1930 by Jakob Erdheimand William Chester, approximately 1500 cases have been reportedworld-wide. Despite the majority of literature comprised by casereports, a predilection for males in their 5th and 7th decade of life withmultisystem involvement that may include dermatologic systems,central nervous system, skeletal, cardiovascular, renal systems havebeen frequently reported. The presenting symptoms most commonlyinclude fatty nodules on the eyelids (xanthelasma) and cutaneousxanthomas-like lesions of the skin, proptosis, diabetes insipidus,dysarthria, headache, lower extremity bone pain and imbalance,although many others have been described.

AB - Erdheim-Chester Disease (ECD) is a rare form of non-Langerhans-cell histiocytosis. Since its first description in 1930 by Jakob Erdheimand William Chester, approximately 1500 cases have been reportedworld-wide. Despite the majority of literature comprised by casereports, a predilection for males in their 5th and 7th decade of life withmultisystem involvement that may include dermatologic systems,central nervous system, skeletal, cardiovascular, renal systems havebeen frequently reported. The presenting symptoms most commonlyinclude fatty nodules on the eyelids (xanthelasma) and cutaneousxanthomas-like lesions of the skin, proptosis, diabetes insipidus,dysarthria, headache, lower extremity bone pain and imbalance,although many others have been described.

M3 - Presentation

T2 - Inaugural 2020 San Diego Dermatology Symposium

Y2 - 11 September 2020 through 13 September 2020

ER -