Results 91 to 100 of about 29,211 (229)
Erdheim Chester disease: A case with cutaneous involvement
Turkderm Turkish Archives of Dermatology and VenereologyErdheim-Chester disease (ECD) is a rare multisystem disease characterized by the proliferation of non-Langerhans histiocytes. It is characterized by excessive production and accumulation of histiocytes in multiple tissues and organs. Sites of involvement
Sera Nur Yücesoy +7 more
doaj +1 more source
Histiocytic syndromes in children.
The Turkish journal of pediatrics, 1997 The "histiocytes" are a group of proliferative disorders of the mononuclear phagocyte system whose etiologies are basically unknown. The majority of childhood histiocytoses are expressions of excessive numbers of Langerhans cells, representing so-called Langerhans cell histiocytosis.
Cetingul, N +5 more
openaire +3 more sources
What Is Your Diagnosis? Multiple Subcutaneous Lumps in a Horse
Veterinary Clinical Pathology, EarlyView.
Federica Meistro +4 more
wiley +1 more source
What Is Your Diagnosis? Blood Smear From a Mixed‐Breed Dog
Veterinary Clinical Pathology, EarlyView.
Laura S. Peres +5 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 8, August 2026.ABSTRACT HLH must be suspected in liver transplant patients who exhibit fever, cytopenia, hyperferritinemia, and dysfunction of the graft. HLH‐2004 guidelines and H‐score assessment early on will aid in early diagnosis and management, although prognosis remains poor when there are opportunistic infections.
Saif Ali Malik +5 more
wiley +1 more source
Peritoneal Tuberculosis Presenting as Massive Ascites in Pregnancy: A Case Report
Clinical Case Reports, Volume 14, Issue 8, August 2026.ABSTRACT Abdominal tuberculosis, especially peritoneal tuberculosis, is uncommon in pregnancy. The diagnosis during pregnancy is a challenge due to many signs and symptoms being nonspecific and mimicking the symptoms of pregnancy. The presence of ascites, with anorexia and weight loss in pregnancy from endemic regions, should be addressed with ...
S. Gyamtsho, S. Dechen, S. Choden
wiley +1 more source
Juvenile Xanthogranuloma With Hydrocephalus
Indian Journal of Dermatology, 2004 Juvenile xanthogranuloma (JXG) is a rare, benign, self-healing tumor of unknown etiology arising from non-Langerhans†cell histiocytes.
Ghosh Arghyaprasun +4 more
doaj
Hematological Oncology, Volume 44, Issue 5, September 2026.
Jerome Razanamahery +10 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 8, August 2026.ABSTRACT Adult‐onset Still's disease (AOSD) is a rare systemic autoinflammatory condition that presents with symptoms such as episodic fevers, a transient rash, inflammatory arthritis, and significant systemic inflammation. Diseases that have a relapsing–remitting clinical course can be challenging to diagnose and treat. We present a case of an 18 year
Tasnim Nafian +4 more
wiley +1 more source