Results 61 to 70 of about 7,474 (152)

Langerhans' cell histiocytosis of the frontal bone [PDF]

, 1994
Con Moshegov, Peter Martin, Philip C. Myers, Marijan Fïlipic   +3 more
openalex   +1 more source

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

Primary Langerhans Cell Histiocytosis of the Vulva [PDF]

, 1993
K. Voelklein, H.-P. Horny, K. Marzusch, J. Dietl   +3 more
openalex   +1 more source

Radiologic manifestation of pulmonary Langerhans' cell histiocytosis [PDF]

, 1993
Jong Sung Kim, Duk Ja Bang, Hyun Chul Rhim, Seok Chol Jeon, Seung Ro Lee, Chang Kok Hahm   +5 more
openalex   +1 more source

Langerhans’ cell histiocytosis diagnosed due to dermatological perianal lesion

Journal of Coloproctology, 2017
Langerhans’ cell histiocytosis is a rare disease characterized by proliferation of Langerhans cells in the body. It affects mainly males, predominantly in childhood. Ulcerated plaques are one of the cutaneous forms of presentation.
Bruno Lorenzo Scolaro, Gustavo Becker Pereira, Daniel Cury Ogata, Fernanda Souto Padrón Figueiredo Vieira da Cunha, Ana Cristina Martins Effting, Rafael Oselame Guanabara   +5 more
doaj   +1 more source

Langerhans cell histiocytosis of the sacrum

Radiology Case Reports, 2014
Langerhans cell histiocytosis is a rare disease with a wide spectrum of clinical presentations. It is a multisystemic disease with organ system involvement ranging from simple-where it involves only one organ-to widespread progressive disease. Although it can affect any age group, the peak incidence is between 1 and 3 years of age.
openaire   +4 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

Recurrence of recipient Langerhans' cell histiocytosis following bilateral lung transplantation [PDF]

, 1998
Shahid Habib, Johnson Yates Congleton, Denis H. Carr, Judith Partridge, B Corrin, DM Geddes, Nicholas R. Banner, Magdi H. Yacoub, Margaret Burke   +8 more
openalex   +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

Hypothalamo-Pituitary Abnormalities in Adult Patients with Langerhans Cell Histiocytosis: Clinical, Endocrinological, and Radiological Features and Response to Treatment [PDF]

, 2000
Gregory Kaltsas, Thomas Powles, Jane Evanson, P N Plowman, J. E. Drinkwater, P Jenkins, JP Monson, G. M. Besser, Ashley Grossman   +8 more
openalex   +1 more source