Results 191 to 200 of about 9,549 (243)

A clinical study incorporating multimodal ¹⁸F-FDG PET/CT metabolic parameters, genetic markers, and clinical characteristics for the evaluation and prediction of treatment efficacy and prognosis in Langerhans cell histiocytosis. [PDF]

Front Med (Lausanne)
Huang Z, Qi W, Rao T, Zeng Q, Lu P, Zhang J, Qiu Z, Xiao G, Liu Q, Fu H, Liao F.   +10 more
europepmc   +1 more source

Merkel cell polyomavirus DNA sequences in tissue from a patient with Histiocytosis. [PDF]

J Clin Exp Hematop
Murakami I, Yorita K, Hashida Y, Daibata M, Yoshino T.   +4 more
europepmc   +1 more source

An unusual case of non-Langerhans cell histiocytosis [PDF]

Journal of the American Academy of Dermatology, 1994
A 28-month-old boy had firm, red nodules for 4 months that were mostly localized to the face. The eruption was preceded by conjunctivitis, eyelid edema, and swelling of the root of the nose. He also had dyspnea, anisocoria with areflexia, swelling of the parotid glands, and hepatosplenomegaly. A bone marrow aspirate showed 25% eosinophils.
Ramon Grimalt, E. Ermacora, Dario Portaleone, Ruggero Caputo, Stefano Cavicchini   +4 more
openaire   +2 more sources

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Non-Langerhans cell histiocytosis

Acta Neurologica Belgica, 2016
A 34-year-old man complained of seizures, headache and reduced visual acuity for a month. Physical examination revealed intracranial hypertension. CSF showed high opening pressure, increase of protein (121 mg/dl) and 26 leukocytes per mm, 94 % of which were lymphomononuclear cells, with cytoplasmic and nuclear atypia.
Lívia Nathália Alaite Silveira, Luciano de Souza Queiroz, Fabiano Reis   +2 more
openaire   +2 more sources

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 M. Chou, Elaine Morgan, Anthony J. Mancini   +3 more
openalex   +4 more sources

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
R. de Groot, M. E. F. Prins, V. D. Vuzevski, Arnold P. Oranje   +3 more
openaire   +3 more sources

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, M. Simon, Walter H. C. Burgdorf   +3 more
openalex   +4 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   +3 more sources