Sivasubramanian Dhiran, Balasubramanian Karthick, Mohamed Kalifa Mohamed Raghib Hussain, Sanil Sathwik, Aravind Smrti, Palanisamy Nithish Nanda, Senthilkumar Virushnee
Department of Cardiology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA.
Department of Critical Care Medicine Christian Medical College Vellore India.
Respirol Case Rep. 2025 Jun 10;13(6):e70237. doi: 10.1002/rcr2.70237. eCollection 2025 Jun.
Erdheim-Chester Disease (ECD) is an extremely rare, non-Langerhans cell histiocytosis characterised by the proliferation of foamy histiocytes infiltrating various organs. It almost always presents with osteosclerosis of the long bones, making our case atypical due to the absence of skeletal involvement despite widespread infiltration of other organs.
厄尔德海姆-切斯特病(ECD)是一种极其罕见的非朗格汉斯细胞组织细胞增多症,其特征为泡沫状组织细胞增殖并浸润各种器官。该病几乎总是伴有长骨骨硬化,而我们的病例因尽管其他器官广泛浸润但无骨骼受累而显得不典型。