Results 131 to 140 of about 6,841 (183)

A Child with Both Langerhans and Non‐Langerhans Cell Histiocytosis

Pediatric Dermatology, 2002
Abstract: The histiocytic syndromes consist of a group of disorders that share in common the proliferation of cells of the monocytic/macrophage lineage. It has been conventional to divide the histiocytoses into two separate groups: Langerhans cell histiocytosis (LCH) and non‐LCH.
Ayelet, Shani-Adir, Pauline, Chou, Elaine, Morgan, Anthony J, Mancini   +3 more
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Congenital self-healing non-Langerhans cell histiocytosis

European Journal of Pediatrics, 1988
Clinical, morphological, ultrastructural and immunological studies were performed in a case of congenital self-healing non-Langerhans cell histiocytosis. The patient showed several aspects that have not been published before: a large nodule in the vulvar region, vesiculobullous elements and pneumonia (asymptomatic). The relationship of the vesicles and
A P, Oranje, V D, Vuzevski, R, de Groot, M E, Prins   +3 more
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Progressive nodular histiocytosis – rare variant of cutaneous non‐Langerhans cell histiocytosis

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2006
SummaryProgressive nodular histiocytosis is an extremely rare skin disease is clinically characterized by the coincidence of two distinct lesions, namely, superficial xanthomatous papules up to 5 mm and deep nodules and tumors 1–3 cm. Histologically the nodules represent spindle cell xanthogranulomas.
Matthias, Lüftl, Heidi, Seybold, Miklós, Simon, Walter, Burgdorf   +3 more
openaire   +2 more sources

Progressive Histiocytosis: Description of a Case of Slow-Course Non-Langerhans Cell Histiocytosis

Dermatology, 2002
We describe the case of a 37-year-old male patient who in 1992 started developing a skin eruption characterized by dark red to red-yellow papulonodular lesions that showed no tendency to spontaneous resolution. Visceral organs were not involved and the lipid pattern was basically normal.
R, Caputo, A, Brezzi, G, Vaccari, S, Cavicchini, R, Gianotti   +4 more
openaire   +2 more sources

Endolymphatic Non-Langerhans Cell Histiocytosis of the Larynx

Journal of Pediatric Hematology/Oncology, 2010
We report on an uncommon laryngeal non-Langerhans cell histiocytosis. An 11-year-old boy presented with a 6 months history of progressive breath inhibition. Magnetic resonance imaging showed diffuse laryngeal and local lymph node swelling. Histology first resembled sarcoidosis, however, corticosteroids were ineffective.
Carl Friedrich, Classen, Dieter, Haffner, Horst, Nizze, Peter, Möller, Friedrich, Prall   +4 more
openaire   +2 more sources

Primary cerebral non-Langerhans cell histiocytosis: MRI and differential diagnosis

Neuroradiology, 2002
We report a young woman with primary cerebral non-Langerhans cell histiocytosis of the juvenile xanthogranuloma family. The clinical course was complicated by extensive infiltration of cranial nerves and meninges and epi- and intramedullary spinal dissemination.
U, Ernemann, M, Skalej, M, Hermisson, M, Platten, R, Jaffe, K, Voigt   +5 more
openaire   +2 more sources

Fibroblastic rheumatism: fibromatosis rather than non‐Langerhans cell histiocytosis

Journal of Cutaneous Pathology, 2010
Background: Fibroblastic rheumatism is a unique fibro‐proliferative disease affecting the skin and joints. It is characterized by distinctive clinical and histological features related to benign spindle‐shaped cells proliferation. Pediatric reports are scarce in the literature.
Nicolas, Kluger, Alexandra, Dumas-Tesici, Dominique, Hamel, Nicole, Brousse, Sylvie, Fraitag   +4 more
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Intracranial non-Langerhans cell histiocytosis presenting as an isolated intraparenchymal lesion

Pediatric Radiology, 2010
Non-Langerhans cell histiocytosis in the absence of cutaneous or other organ involvement is very rare. A Caucasian boy age 3 years 11 months presented with episodes of recurrent right-side seizures over 2 weeks. Brain CT and MR imaging showed a single enhancing left frontal lobe lesion.
Smitha, Rajaram, Stephen B, Wharton, Fiona, Shackley, Ashok, Raghavan, Daniel J A, Connolly   +4 more
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Non Langerhans Cell Histiocytosis of the Rectum: Case Report and Review of the Literature

Japanese Journal of Gastroenterology and Hepatology, 2022
Histiocytosis is a condition resulting from the abnormal proliferation of dentritic cells of the mononuclear phagocytic system. Previously classified as Langerhans cell histiocytosis and non-Langerhans cell histiocytosis, and recently into 5 categories (L, C, R, M and H), it can be localized to an organ or have a systemic manifestation, affecting most ...
Bouhairie MM, Mansour J, El Naderi S, Abou Rached A   +3 more
openaire   +1 more source

New entity of an isolated pulmonary non-Langerhans cell histiocytosis

European Respiratory Journal, 2013
Background: Histiocytic disorders are rare, heterogeneous diseases with abnormal tissue infiltration by histiocytes. So far, pulmonary manifestation in Non-Langerhans cell histiocytoses (NLCH) occurred only as a part of a systemic disease. Case: A 37 year old male stonesculptor suffered from progressive dyspnea and thoracic tightness.
Michael Kreuter, Claus Peter Heussel, Christian Nagel, Richard P. Baum, Philipp A. Schnabel, Felix J.F. Herth, Dirk Theegarten   +6 more
openaire   +1 more source