Results 11 to 20 of about 8,935 (206)
Langerhans Cell Histiocytosis Presenting With Diabetes Insipidus in a 2 Years Old Child: A Case Report. [PDF]
Clin Case RepABSTRACT This case report highlights that Langerhans cell histiocytosis should be suspected in the differential diagnosis for children who exhibit failure to thrive, diabetes insipidus, and skin lesions. Early recognition and timely management are crucial for preventing irreversible hypothalamic–pituitary damage and improving outcomes.
Yohannes KG +3 more
europepmc +2 more sources
ALK-Positive Histiocytosis With Unilateral Breast Involvement: A Case Report. [PDF]
Clin Case RepABSTRACT APH is a rare disorder characterized by the proliferation of ALK‐expressing histiocytes with variable anatomical involvement; however, mammary involvement is exceptionally rare. A 32‐year‐old woman presented with a painless right breast mass. Ultrasound identified a 9 × 8 mm hypoechoic nodule, categorized as BI‐RADS 4A.
Liu X, Ren D, Liang Y.
europepmc +2 more sources
Histiocytosis X and Bronchopulmonary Adenocarcinoma: A Rare Coexistence
Canadian Respiratory Journal, 2002 There exists a rarely observed association between pulmonary histiocytosis X and bronchopulmonary cancer. However, the frequency of bronchopulmonary cancer in these patients is higher than in the general population.
Akýn Kaya +5 more
doaj +1 more source
Hand-Schüller-Christian disease
Indian Journal of Dental Research, 2012 Langerhan cell histiocytosis, formerly known as histiocytosis X, traditionally denotes a group of diseases that stem from proliferative reticuloendothelial disturbances.The etiology and pathogenesis of the disease remain debatable.
Deepak Bhargava +3 more
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Histiocytosis x: Recurrent isolated mandibular lesion (case report) [PDF]
Stomatološki glasnik Srbije, 2003 Histiocytosis X usually affects children and adolescents. In our case, a 54-year-old woman was admitted to hospital for evaluating and treatment of an isolated, painless swelling of the left side of the mandible.
Basta-Jovanović Gordana M. +3 more
doaj +1 more source
Journal of Medical Case Reports, 2019 Background Langerhans cell histiocytosis previously known as histiocytosis X is a rare disease of children and young adults with a very broad clinical spectrum. In children, its annual incidence is estimated between 0.2–0.5 per 100,000.
Salahoudine Idrissa +6 more
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HYSTYOCYTOSIS X: VERIFICATION OF DIAGNOSIS
Vestnik Dermatologii i Venerologii, 2018 A clinical case of histiocytosis X, rarely found in the practice of a dermatovenereologist, is described, the pathognomonic clinical symptoms of this dermatosis, including skin lesions, that occur in 50 to 80 % of cases of all forms are displayed.
V. V. Starostenko +3 more
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Vulvar Langerhans cell histiocytosis: a case report
The Pan African Medical Journal, 2014 Langerhans cell histiocytoses (LCH) are a rare group of disorders that comprise a large spectrum of diseases initially known as histiocytosis X. In this case report, we relate a case of LCH affecting the vulva of a 47-year-old female.
Nadia Khoummane +3 more
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Contemporary Clinical Dentistry, 2019 Langerhans cell histiocytosis (LCH) is a rare hematological disorder characterized by local or generalized, uncontrolled proliferation and infiltration of Langerhans type of histiocytic cells.
Richa Nangalia +3 more
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Giant Cell Lesion or Langerhans' Cell Histiocytosis of the Mandible? A Case Report
European Journal of Inflammation, 2012 Langerhans' cell histiocytosis (LCH), formerly known as histiocytosis X, is characterized by cell proliferation. The leading clinical symptom of LCH within mandibular and maxillary bones is pain and it may resemble periodontal diseases, apical cysts ...
V. Valentini +6 more
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