Create issue ticket

1,014 Possible Causes for Langerhans Cell Histiocytosis, Pediatric Disorder

  • Pulmonary Histiocytosis X

    Pulmonary Langerhans Cell Histiocytosis (PLCH) Eosinophilic Granuloma of the Lung Pulmonary Langerhans Cell Granulomatosis Pulmonary Histiocytosis X Uncommon ILD Young adults[] PLCH is similar to pediatric histiocytic disorders (Letterer-Siwe disease and Hand-Sch ü ller-Christian disease).[] Contemporary classification of histiocytic disorders. Med Pediatr Oncol 1997;29:157–166PMID : 9212839. 6. Brauner MW, Grenier P, Mouelhi MM, Mompoint D, Lenoir S.[]

  • Langerhans-Cell Histiocytosis

    Langerhans cell histiocytosis (LCH), also called Histiocytosis X, is a rare disease characterized by the proliferation and accumulation of Langerhans cells in various tissues[] Ting-Wen An Lee, Radhika Muzumdar and Paul Saenger, Growth Disorders, Textbook of Clinical Pediatrics, 10.1007/978-3-642-02202-9_386, (3739-3757), (2012).[] Langerhans cell histiocytosis is occasionally misspelled as "Langerhan" or "Langerhan's" cell histiocytosis, even in authoritative textbooks.[]

  • Eosinophilic Granuloma

    A case of unifocal Langerhans' cell histiocytosis or eosinophilic granuloma in a child is reported where the frontal, zygomatic and maxillary bones of the left orbital wall[] disorder.[] Eosinophilic granuloma is the localized and most benign form of Langerhans' cell histiocytosis.[]

  • Interstitial Pulmonary Fibrosis of the Newborn

    Cell Histiocytosis (LCH) is a rare disease 2008-2018 MeDitorial ISSN 1803-6597 Last update: 25.3.2018 Statement[] Skin disorders caused by fungi. In: Paller AS, Mancini AJ, eds. Hurwitz Clinical Pediatric Dermatology. 5th ed. Philadelphia, PA: Elsevier; 2016:chap 17.[] Disorders of the sweat glands. In: Nelson Textbook of Pediatrics. 20th ed. Philadelphia, Pa.: Elsevier; 2016. . Accessed July 29, 2016. Kalra MG, et al.[]

  • Thrombocytopenia-Absent Radius Syndrome

    We describe a child with thrombocytopenia-absent radius (TAR) syndrome in whom a refractory Langerhans cell histiocytosis (LCH) developed at 9 years.[] Murray Thrombocytopenia in the newborn Curr Opin Pediatr, 15 (2003), pp. 17-23 [20.] L.V. Black, A.[] We report here on a child affected by TAR syndrome associated with Langerhans cell histiocytosis.[]

  • Velocardiofacial Syndrome

    Behavior, brain, and genome in genomic disorders: Finding the correspondences. Journal of Developmental and Behavioral Pediatrics, 31, 602–609.[] He is Professor of Otolaryngology and Professor of Pediatrics at Upstate.[] Similarly, specially trained pediatric cardiologists can look carefully at the heart of a developing fetus in order to detect serious heart defects.[]

  • Protein-Losing Enteropathy

    Abstract Protein-losing enteropathy (PLE) is frequently complicated in patients with gastrointestinal tract-involved Langerhans cell histiocytosis (LCH); however, LCH per[] PLE is a complication of a disorder, be it lymphatic obstruction or mucosal injury.In pediatric protein losing enteropathy there are several changes in epithelial cells causing[] Langerhans cell histiocytosis protein-losing enteropathy hemophagocytic syndrome infants Accepted November 12, 2009.[]

  • Congenital Alopecia

    Atypical clinical features may mimic impetigo, Langerhans cell histiocytosis, and carcinoid syndrome; however, only 1 case of scarring alopecia associated with mastocytosis[] A certification by the Board of Dermatology; practitioners treat pediatric and adult patients with disorders of the skin, mouth, hair and nails as well as a number of sexually[] Frieden, two of the most important names in the fields of dermatology and pediatrics.[]

  • Scabies

    Langerhans cells histiocytosis (LCH) affecting the skin most commonly has clinical and histopathologic diagnostic features.[] In nodular scabies, lesions may be clinically or histologically misdiagnosed as Langerhans cell histiocytosis, insect bite reaction, non-Langerhans cell histiocytosis, lymphoma[] Yoon Seok Yang, Yun Sun Byun, Jin Hye Kim, Hye One Kim and Chun Wook Park, Infantile Scabies Masquerading as Langerhans Cell Histiocytosis, Annals of Dermatology, 27, 3, ([]

  • Congenital Cortical Hyperostoses

    cell histiocytosis Other clavicle abnormalities found only in infancy and childhood birth fracture: see birth trauma infantile cortical hyperostosis (Caffey disease) congenital[] cell histiocytosis (.66) Larsen syndrome (multiple congenital dislocations) (.1626) Laurence-Moon-Bardot-Biedel syndrome (syndactyly, mental retardation, obesity)(4.1894)[] […] tumor, Langerhans cell histiocytosis, or even an osteolytic metastasis on radiographs. [7] The increased fat in this region can be readily seen on MRI and helps make the[]

Further symptoms

Similar symptoms