Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues.

Hamartoma

A disordered proliferation of mature tissues that is native to the site of origin, e.g., exostoses, nevi and soft tissue hamartomas. Although most hamartomas are benign, some histologic subtypes, e.g., neuromuscular hamartoma, may proliferate aggressively such as mesenchymal cystic hamartoma, Sclerosing epithelial hamartoma, Sclerosing metanephric hamartoma.


Total: 3

                      


(per page)
PMID (PMCID)
21225516
MIXED_SAMPLE Adult
Rare primary tumours of the hypothalamus in adults: clinical course and surgical treatment.
Majchrzak K, Bierzynska-Macyszyn G, Bobek-Billewicz B, Majchrzak H, Ladzinski P.
Neurol Neurochir Pol. 2010;44(6):546-53.
There were 2 patients with craniopharyngiomas located exclusively in the third ventricle, and single patients with gemistocytic astrocytoma, Langerhans cell histiocytosis X and hamartoma of the hypothalamus each.
21225516
MIXED_SAMPLE Adult
Rare primary tumours of the hypothalamus in adults: clinical course and surgical treatment.
Majchrzak K, Bierzynska-Macyszyn G, Bobek-Billewicz B, Majchrzak H, Ladzinski P.
Neurol Neurochir Pol. 2010;44(6):546-53.
There were 2 patients with craniopharyngiomas located exclusively in the third ventricle, and single patients with gemistocytic astrocytoma, Langerhans cell histiocytosis X and hamartoma of the hypothalamus each.
15389309
MIXED_SAMPLE Infant
Clinico-pathological conference 2002.
Odell EW, Aldred M, Carlos R, Curran A, Heikinheimo K, Hille J, Ho KH, Kratochvil FJ, Lau SH, Murrah V, Reichart P, Sood A, Tanaka Y, Tilakaratne WM, Yih WY.
Ann Acad Med Singapore. 2004;33(4 Suppl):53-8.
Case diagnoses included a large, possibly intraosseous, myofibroma presenting with an oral mass; Langerhans cell histiocytosis with facial skin lesions; an intraosseous vascular hamartoma of the maxilla with worrying radiological features; an unusual mixed radiolucency of the jaw caused by cemento-ossifying fibroma; an osteosarcoma of the posterior mandible causing a well-defined radiolucency and an intraoral squamous cell carcinoma in a child.