1.Neurological Involvement in Erdheim-Chester Disease.
Miriam ALVAREZ-ALVAREZ ; Ronald MACIAS-CASANOVA ; M Angeles FIDALGO-FERNANDEZ ; Jose Pablo MIRAMONTES GONZALEZ
Journal of Clinical Neurology 2016;12(1):115-116
No abstract available.
Erdheim-Chester Disease*
2.Reply to Commentary on "A Case of Erdheim-Chester Disease with Asymptomatic Renal Involvement".
Cancer Research and Treatment 2012;44(4):280-280
No abstract available.
Erdheim-Chester Disease
3.Commentary on "A Case of Erdheim-Chester Disease with Asymptomatic Renal Involvement".
Cancer Research and Treatment 2012;44(4):279-279
No abstract available.
Erdheim-Chester Disease
4.Diagnosis and Treatment of Erdheim-Chester Disease -Review.
Journal of Experimental Hematology 2016;24(4):1256-1259
Erdheim-Chester Disease (ECD) is a rare form of non Langerhans' cell histiocytosis. The etiology of ECD is unknown yet. The disease is characterized by the infiltration of lipid-laden histiocytes with foamy to bones and various organs. The heterogeneous manifestations of ECD vary among different individuals. This results in a presentation that may vary from an indolent focal disease to a life threatening organ failure. This review focuses on the etiology, clinical presentation, diagnostic criteria and treatment of Erdheim-Chester disease (ECD).
Erdheim-Chester Disease
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Humans
5.Erdheim-Chester disease in a child: case report.
Chuan WEN ; Qing-chun LIANG ; Wu-qing WAN
Chinese Journal of Pediatrics 2011;49(3):231-232
7.A Case of Erdheim-Chester Disease with periodic fever and knee pain.
Jong Rak HONG ; Hong Ghi LEE ; Young Hyeh KO ; Joong Mo AHN ; Yeon Hyeon CHOI ; Byung Tae KIM
Korean Journal of Medicine 1999;56(4):542-546
ECD is a rare, non-Langerhans form of histiocytosis. The first case was reported in 1930 by Chester and the term ECD was first described by Jaffe in 1972. Many authors have suggested that ECD is a part of the spectrum of Langerhans cell histiocytosis(LCH), whereas others believe ECD as a distinct lipoidosis because of the symmetric distribution of the long bone lesions on the roentgenogram and the lack of Langerhans granules and S-100 antibody staining in the foamy histiocytes. We experienced a case of Erdheim-Chester disease (ECD) with periodic night fever, myalgia and both knee pain, the first case reported in Korea.
Erdheim-Chester Disease*
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Fever*
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Histiocytes
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Histiocytosis
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Knee*
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Korea
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Lipidoses
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Myalgia
10.Erdheim Chester Disease (ECD): A Case Report.
Jin Ho LEE ; Sung Taek JUNG ; Yoo Duk CHOI
The Journal of the Korean Bone and Joint Tumor Society 2013;19(1):28-32
Erdheim Chester disease (ECD) is very rare non-Langerhans cell histiocytosis (LCH) which occurs in the skeletal system and multiple organs. As it is progressive, sometimes it causes fatal results. However, it is often misdiagnosed as LCH or multiple bone metastasis and, thus, is very difficult to diagnose. In Korea, only 10 cases were first reported in 1999. In particular, there have been a few orthopedic approaches or reports in English-speaking literatures, and no report has been issued in Korea. The authors performed bone biopsy in patients with knee and lower extremity pain who were referred for the integrated treatment. We attempts to report this diagnosis experience with literature review.
Biopsy
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Erdheim-Chester Disease
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Histiocytosis
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Histiocytosis, Langerhans-Cell
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Humans
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Knee
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Korea
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Lower Extremity
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Neoplasm Metastasis
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Orthopedics