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Erdheim-Chester Disease with Perirenal Masses Containing Macroscopic Fat Tissue

Byeon J, Kim KA, Hwang SS, Park SY, Kim HA

Erdheim-Chester disease is a rare non-Langerhans-cell histiocytosis involving multiple organs. On histological evaluation, lipid-laden histiocyte aggregates in Erdheim-Chester disease is detected, but fat tissue in affected organs is not noted...
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Commentary on "A Case of Erdheim-Chester Disease with Asymptomatic Renal Involvement"

Li Cavoli

  • KMID: 1804890
  • Cancer Res Treat.
  • 2012 Dec;44(4):279-279.
No abstract available.
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Reply to Commentary on "A Case of Erdheim-Chester Disease with Asymptomatic Renal Involvement"

Lee HJ, Kim TM

  • KMID: 1804891
  • Cancer Res Treat.
  • 2012 Dec;44(4):280-280.
No abstract available.
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A Case of Erdheim-Chester Disease with Bilateral Hydronephrosis

Lee W, Park NC

  • KMID: 2292341
  • Korean J Urol.
  • 2001 Apr;42(4):453-456.
Erdheim-Chester disease (ECD) is a disseminated xanthogranulomatous infiltrative disease of unknown origin which reveals the infiltration of different organs and bones by foamy histiocytes. Patients with ECD have specific skeletal...
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Intracranial Erdheim-Chester Disease

Yoo NH, Yee GT, Choi CY, Whang CJ

  • KMID: 1588732
  • J Korean Neurosurg Soc.
  • 2004 Dec;36(6):496-498.
Erdheim-Chester disease is a rare form of non-Langerhans cell histiocytosis consisting of disseminated xanthogranulomatous infiltration and fibrosis that involves the long bones, visceral organs, orbital, retroperitoneal and soft tissues. Intracranial...
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A Case of Erdheim-Chester Disease Mimicking Systemic Lymphangitic Metastasis

Sim YS, Park JK, Lee JH, Song DE, Chang JH

  • KMID: 2259297
  • Korean J Med.
  • 2011 Jun;80(6):712-717.
Erdheim-Chester disease (ECD) is non-Langerhans cell histiocytosis that leads to multi-organ involvement with unknown etiology. We report a 64-year-old woman with a dry cough and dyspnea. She had interlobular septal...
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A case of Erdheim-Chester disease that presented with chronic renal failure

Hwang HS, Ji BS, Lee CK, Kim JY, Choi BS, Yang CW, Kim YS

  • KMID: 2305923
  • Korean J Med.
  • 2007 Aug;73(2):216-222.
Erdheim-Chester disease is a rare non-langerhans cell histiocytic disorder of an unknown cause that may associate with multisystem, rapidly fatal, infiltrative disease. We report here on a case of Erdheim-Chester...
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Neurological Involvement in Erdheim-Chester Disease

Alvarez-Alvarez M, Macias-Casanova R, Fidalgo-Fernandez MA, Miramontes Gonzalez JP

No abstract available.
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A Case of Erdheim-Chester Disease with periodic fever and knee pain

Hong JR, Lee HG, Ko YH, Ahn JM, Choi YH, Kim BT

  • KMID: 2143117
  • Korean J Med.
  • 1999 Apr;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...
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Successful Treatment of Erdheim-Chester Disease with Multisystemic Involvement in a 4-year-old Child by Interferon-α and Corticosteroid

Hwang JW, An CH, Lee MK, Hwang PH

Erdheim-Chester disease (ECD) is a rare form of proliferative non-Langerhans cell histiocytosis that involves multiple organs and is associated with a high mortality. The prognosis of ECD is variable, and...
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A Case of Cerebral Erdheim-Chester Disease With Progressive Cerebellar Syndrome

Na SJ, Lee KO, Kim JE, Kim YD

Erdheim-Chester disease (ECD) is a rare non-Langerhans form of histiocytosis. Cerebellar involvement is rare in this syndrome. We report a 37-year-old woman with slowly progressive cerebellar ataxia, dysmetria of limbs,...
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Improvement of Erdheim-Chester disease-related renal failure after treatment with anakinra

Podesta MA, Graziani G, Reggiani F, Buemi M, Badalamenti S, Ponticelli C

Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis characterized by infiltrates of lipid-laden CD68+/CD1- histiocytes, affecting heart, lungs, central nervous system, and bones. Kidney and adjacent structures can also...
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Erdheim-Chester Disease Presenting as an Anterior Mediastinal Tumor without Skeletal Involvement

Lee K, Kim HR, Roh J, Ok YJ, Jeon BB, Kim YW

Erdheim-Chester disease (ECD) is a form of non–Langerhans cell histiocytosis that most commonly involves the skeletal system. We report an unusual case of ECD presenting as an anterior mediastinal tumor...
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A Case of Erdheim-Chester Disease with Laryngeal Involvement

Park JS, Moon MG, Lee JH, Lee SH

Erdheim-Chester disease (ECD) is a rare form of non-Langerhans cell histiocytosis with multi-organ involvement. Bones, cardiovascular system, central nervous system, kidney, skin and many different organs can be involved but...
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Erdheim Chester Disease (ECD): A Case Report

Lee JH, Jung ST, Choi YD

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,...
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A Case of Erdheim-Chester Disease Developed during Treatment of Leukemia in a Child

Hong JP, Ahn WK, Lim JY, Jung JE, Hahn SM, Han JW, Lyu CJ

Erdheim-Chester disease (ECD) is a rare non-Langerhan's cell histiocytosis disorder characterized by replacement of normal tissue by lipid-laden histiocytes affecting various organs. A few pediatric cases have been reported worldwide....
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Erdheim-Chester Disease with Emperipolesis: A Unique Case Involving the Heart

Zhu P, Li N, Yu L, Miranda MN, Wang G, Duan Y

Histiocytosis is an uncommon disease characterized by excessive accumulation of histiocytes. Here, we report a rare case of non-Langerhans-cell histiocytosis in a 51-year-old woman who presented with severe symptoms of...
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Erdheim-Chester Disease with Hepatitis, Glomerulonephritis, Aplastic Anemia and Lung Involvement

Park JW, Chung CU, Shin JY, Jung SY, Yoo SJ, Lee JE, Jung SS, Kim JO, Kim SY, Park HS

  • KMID: 2319256
  • Tuberc Respir Dis.
  • 2009 Oct;67(4):345-350.
Erdheim-Chester disease (ECD) is a proliferative non-Langerhans cell histiocytosis of multiple organs. This is a rare disease of unknown etiology with a high mortality. We present the case report of...
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Erdheim-Chester Disease: Two Cases of Orbital Involvement

Kim YJ, Kim YD

  • KMID: 2206126
  • J Korean Ophthalmol Soc.
  • 2002 Jul;43(7):1323-1329.
PURPOSE: ECD is a rare idiopathic condition characterized by infiltration of the bone, heart, lungs, retroperitoneum, skin, CNS and other tissues by a fibrosing process containing xanthomatous histiocytes and multinucleated...
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A Case of Erdheim-Chester Disease Who Has Policythemia Vera

Kim JE, Lee HJ, Rhee CK, Yoon HK, Song JS

Erdheim-Chester disease (ECD) is a rare disease that is characterized by multi-organ involvement of foamy histiocytes. It causes systemic inflammation, and also demonstrates various clinical manifestations and has a poor...
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