Results 101 to 110 of about 4,921,178 (191)

A case of coexisting Warthin tumor and langerhans cell histiocytosis associated with necrosis, eosinophilic abscesses and a granulomatous reaction in intraparotid lymph nodes

Rare Tumors, 2011
We present a patient (50-year-old male) with coexisting Warthin tumor and involvement of two intraparotid lymph nodes by Langerhans cell histiocytosis associated with necrosis, eosinophilic abscesses and a granulomatous reaction.
Char Loo Tan, Gangaraju Changal Raju, Fredrik Petersson   +2 more
doaj   +1 more source

Langerhans Cell Histiocytosis in a Newborn

Journal of the Chinese Medical Association, 2009
A full-term female baby was admitted to our hospital at the postnatal age of 37 days with generalized vesiculopapular, crateriform skin lesions. Physical examination revealed a well-nourished baby without fever, hepatosplenomegaly or lymphadenopathy. Laboratory examination was normal except for thrombocytosis (platelet count, 970 x 10(3)/microL).
Yang, Tzu-Ying, Chen, Shu-Jen, Yang, Ling-Yu, Tang, Ren-Bin   +3 more
openaire   +2 more sources

Langerhans Cell Histiocytosis of the Clavicle in a 13-Year-Old Boy

Case Reports in Orthopedics, 2014
Langerhans Cell Histiocytosis (LCH) is a rare neoplasm characterized by abnormal proliferation of histiocytic cells. In this case report, we describe a unique case of a 13-year-old boy who presented to the clinic with an insidious onset of mid-clavicular
Shital N. Parikh, Vishal R. Desai, Anita Gupta, Christopher G. Anton   +3 more
doaj   +1 more source

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

Solitary Langerhans cell histiocytosis of the hard palate: a diagnostic pitfall

, 2016
Langerhans cell histiocytosis (LCH) is a relatively rare and unique disease characterized by an abnormal proliferation of immature dendritic cells. It is predominantly seen in children with adults showing less than ten times the incidence compared to ...
Varsha, Dalal, Varsha, D, Siraj, Fouzia, Kaur, M, Kaur, Manveen, Chaudhary, N, Siraj, F, Chaudhary, Neena   +7 more
core   +1 more source

Intestinal Langerhans cell histiocytosis presenting with symptoms similar to inflammatory bowel disease: a case report

Pathology and Oncology Research
Background:Langerhans cell histiocytosis is a rare disease characterized by the abnormal proliferation of Langerhans cells within a single organ or multiple organs.
Yuqing Liu, Zhenwei Chen, Lu Wang, Baizhou Li   +3 more
doaj   +1 more source

Paediatric Langerhans cell histiocytosis with diabetes insipidus: remarkable recovery journey

Journal of the Pakistan Medical Association
A rare condition known as Langerhans cell histiocytosis (LCH) is characterised by the clonal growth of dendritic cells called Langerhans cells, which play a significant role in the immune system. A diverse range of clinical presentations are probable as
Versha Rani Rai, Zulqarnain Buriro, Roshia Parveen, Mohsina Noor, Heeranand Rathore   +4 more
doaj   +1 more source

Langerhans cell histiocytosis: case report

, 2021
Langerhans cells are dendritic cells seen above the basal layer of squamous epithelia. They are cells specialized in the capture of antigens and in the induction of T lymphocyte responses.
Siqueira, Edllanckar dos Santos
core  

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
core   +1 more source

Langerhans cell histiocytosis in monocygote twins: case reports.

, 1996
Langerhans cell histiocytosis includes three clinical forms of histiocytosis X. We describe a disseminated form of Langerhans cell histiocytosis (Letterer-Siwe disease) in monozygotic twins.
Mader I, Stock KW, Steinbrich W, Radue EW   +3 more
core   +1 more source