Results 111 to 120 of about 10,817 (231)

LANGERHANS CELL HISTIOCYTOSIS

, 2005
Ulcerated nodules are often seen in the flexural areas of patients with Langerhans cell histiocytosis, or histiocytosis X (2,5-7). Infants with this condition have widespread cutaneous disease with a seborrheic rash involving the scalp and flexural ...

core   +1 more source

A 50‐year‐old man with a 12‐year history of extensive pachymeningeal thickening

Brain Pathology, Volume 36, Issue 4, July 2026.
Alyssa M. Lee, Siddhartha Gaddamanugu, Kathyrn L. Eschbacher, Aishwarya Ravindran   +3 more
wiley   +1 more source

Erdheim–Chester disease: A multisystem non-Langerhans cell histiocytosis with cutaneous involvement

Journal of the Royal College of Physicians of Edinburgh
Erdheim–Chester disease (ECD) is a rare non-Langerhans cell histiocytosis (LCH) marked by systemic involvement and diverse clinical manifestations. We report a 35-year-old man with yellowish-brown periorbital lesions initially diagnosed as xanthelasma, which later recurred.
Neetu Bhari, Ritu Sharma, Sushant Agrawal, Vishal Gaurav   +3 more
openaire   +2 more sources

Langerhans cell histiocytosis; an institutional study

, 2017
Background: Langerhans cell histiocytosis is a complex rare disease of the dendritic cell system.The disease can occur at any age, with a peak at 5-10 years.
Shovana Karki, Aasia Rajbhandari
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Endocrine manifestations in Langerhans cell histiocytosis.

, 2007
Langerhans cell histiocytosis is a rare, multisystem disease that shows a particular predilection for hypothalamo-pituitary axis involvement. Diabetes insipidus is the most frequent permanent consequence of Langerhans cell histiocytosis, developing in ...
Chrousos, GP, Grossman, AB, Kaltsas, GA, Makras, P, Alexandraki, KI   +4 more
core   +2 more sources

Pulmonary Langerhans' cell histiocytosis (histiocytosis X) following metastasising malignant melanoma

, 2002
Background: Pulmonary Langerhans' cell histiocytosis (histiocytosis X) is an uncommon, diffuse interstitial lung disease of unknown cause, mostly presenting in young smokers.
Mirzaie, Masoud, Tirilomis, Theodor, Dalichau, H., Zenker, Dieter   +3 more
core  

Adult langerhans cell histiocytosis

, 2007
Langerhans cell histiocytosis is a group of idiopathic disorders characterized by the abnormal proliferation of specialized bone marrow-derived Langerhans cells. There are one to two cases per million population.
Bahceci, Mithat, Goekalp, Deniz, Tuzcu, Alparslan, Isikdogan, Abdurrahman, Cil, Timucin   +4 more
core  

Langerhans cell histiocytosis of the thyroid mimicking thyroiditis in a boy: a case report and literature review

BMC Pediatrics
Background Langerhans cell histiocytosis affecting the thyroid commonly presents with nonspecific clinical and radiological manifestations. Thyroid Langerhans cell histiocytosis is typically characterized by non-enhancing hypodense lesions with an ...
Yu Fan Cheng, Ching Che Wang, Pei Shan Tsai, Dao Chen Lin, Wen Hui Huang   +4 more
doaj   +1 more source

A Case of Langerhans Cell Histiocytosis Presenting with Suprasellar Mass and Panhypopituitarism Clinic

Langerhans cell histiocytosis (LCH) is a rare disease involving multiple systems, and it is caused by excessive proliferation of Langerhans cells. The hypothalamic-pituitary region (HPR) is involved in 5%-50% of all LCH patients, particularly those with ...
Murat Şahin, Emek Topuz, Dilek Tüzün, Nursel Yurttutan   +3 more
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Langerhans Cell Histiocytosis (Letterer-Siwe disease ) - Report of a case

, 2011
Langerhans cell histiocytosis is a rare disorder that occurs when there aretoo many of type of white blood cell called a Langerhans cell. We describe a3-months infant girl who developed wide spread skin lesions since she was 4days of age. . The diagnosis
BS Elagraa, Elagraa, BS, El Hassan, AM, MA Abdulla, SI Ayed, Ayed, SI, Abdulla, MA, AM El Hassan   +7 more
core   +1 more source