Results 31 to 40 of about 4,675 (181)

Erdheim-Chester Disease: Case Report

罕见病研究, 2022
Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis characterized by the infiltration of bone and multiple organs by foamy lipid-laden histiocytes. ECD is easy to be misdiagnosed due to its complicated clinical manifestations.
FAN Xiaoyuan, LIU Ting, YOU Hui, SUN Jian, CAO Xinxin, FENG Feng, WANG Fengdan   +6 more
doaj   +2 more sources

Unusual manifestation of Erdheim-Chester disease

BMC Gastroenterology, 2011
Background Erdheim-Chester disease (ECD) is a rare multisystem non-Langerhans cell histiocytosis that is characterized histologically by xanthogranulomatous infiltrates and radiologically by symmetrical sclerosis of long bones.
Schlup Martin, Doyle Terence, Pan Antony, Lubcke Ralf, Schultz Michael   +4 more
doaj   +2 more sources

An unusual Erdheim-Chester disease with orbital involvement: a case report [PDF]

Italian Journal of Medicine, 2016
Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult because
Giuseppe Brunori, Aurelio Seidita, Lydia Giannitrapani, Antonietta Serruto, Francesco Bencivinni, Maurizio Soresi   +5 more
doaj   +2 more sources

Erdheim–Chester disease [PDF]

Clinical Rheumatology, 2010
Erdheim-Chester disease is characterized by long bone pain and symmetric sclerosis of the diametaphyseal portions of the long bones. It is an important differential diagnosis of sclerotic disease of the bones.
Bharath Manu, Akkara Veetil, Harvinder, Luthra   +1 more
  +8 more sources

A case of Erdheim–Chester disease with the BRAF V600E mutation diagnosed via endoscopic sinus surgery [PDF]

, 2023
Erdheim–Chester disease is characterized by the infiltration of foamy histiocytes in tissues. Lesional tissue biopsy is recommended to confirm diagnosis and establish the BRAF mutational status.
Matsuhisa, Takaharu, Tsuyuki, Yuta, Sone, Michihiko, Sato, Juichi, Teranishi, Masaaki   +4 more
core   +1 more source

Erdheim-Chester disease with multisystem involvement evaluated by multimodal imaging: A case report

Radiology Case Reports, 2022
Erdheim-Chester disease is a rare, idiopathic, multisystemic non-Langerhans cell histiocytosis. Little is known about the imaging features. Herein, we report a very uncommon case of Erdheim-Chester disease in a 54-year-old woman with multisystem ...
Jing Liu, MD, Limin Gao, MD, Huaxia Pu, MD, Wenzhang He, MD, Liqing Peng, MD, PhD   +4 more
doaj   +1 more source

Erdheim-Chester Disease: A Rare Presentation With Atrial Flutter and Severe Sinus Node Dysfunction. [PDF]

JACC Case Rep
Alqurashi YG, Al-Qurashi AA, Ajabnoor RM, Althobaiti M, Meer A, Almehmadi F, Al-Qubbany A, Alzahrani A.   +7 more
europepmc   +2 more sources

Apparently isolated CNS involvement in Erdheim-Chester disease: Case report

Radiology Case Reports, 2023
We present the case of a 48-year-old-woman with apparently isolated central nervous system Erdheim-Chester disease characterized by brainstem involvement. Erdheim-Chester disease is extremely rare and multisystem impairment should always be sought in the
Giuseppe Romano, Mario Cirillo, Simona Bonavita, Giuseppe Toro, Andrea Di Pietro, Luigi Lavorgna, Elisabetta Maida, Francesca Pagliuca, Fabrizio Urraro, Cinzia Coppola, Giacomo Lus, Elisabetta Signoriello   +11 more
doaj   +1 more source

Erdheim-Chester disease: misdiagnosed as multiple sclerosis

, 2023
Erdheim-Chester disease is a rare histiocytic neoplasm with a wide range of clinical manifestations. Due to its rarity and protean characteristics, this condition often presents a diagnostic challenge.
Yang, Jason, Khoo, Tien Kheng, Imlay-Gillespie, Louise, Dierkes, Judith Gerarda   +3 more
core   +1 more source

Cardiac and pleuropulmonary involvement in Erdheim-Chester disease without bone lesions: A case report

Radiology Case Reports, 2022
Erdheim–Chester disease is a rare multisystemic non-Langerhans histiocytosis characterized by histiocytes that stain positive for CD68 and negative for CD1a.
Rene Epunza Kanza, MD, PhD, Olivier Houle, MS, Pierre-Luc Simard, MD, Jonathan St-Gelais, MD, Catherine Raymond, MD   +4 more
doaj   +1 more source