Indeterminate cell histiocytosis is a cutaneous condition felt to be caused by dermal precursors of Langerhans cells.
List of articles in "Disease" category - Page 89
Multicentric reticulohistiocytosis
Multicentric reticulohistiocytosis is a multisystem disease beginning usually around the age of 50 years old and is twice as common in women.
Reticulohistiocytoma
Reticulohistiocytoma is a cutaneous condition characterized by a solitary firm dermal skin lesion of less than 1cm in diameter. It usually occurs in young adults or middle aged people most […]
Reticulohistiocytosis
Reticulohistiocytosis is a cutaneous condition of which there are two distinct forms: Reticulohistiocytoma Multicentric reticulohistiocytosis↑
Hereditary progressive mucinous histiocytosis
Hereditary progressive mucinous histiocytosis is an autosomal dominant or X-linked hereditary described on in women.
Papular xanthoma
Papular xanthoma is a cutaneous condition that is a rare form of non-X histiocytosis.
Progressive nodular histiocytosis
Progressive nodular histiocytosis is a cutaneous condition clinically characterized by the development of two types of skin lesions: superficial papules and deeper larger subcutaneous nodules.
Xanthoma disseminatum
Xanthoma disseminatum (also known as Disseminated xanthosiderohistiocytosis and Montgomery syndrome) is a rare cutaneous condition that preferentially affects males in childhood characterized by the insidious onset of small yellow-red to […]
Generalized eruptive histiocytoma
Generalized eruptive histiocytoma (also known as Eruptive histiocytoma and Generalized eruptive histiocytosis) is a rare cutaneous condition characterized by widespread erythematous essentially symmetrical papules particularly involving the trunk and proximal […]
Benign cephalic histiocytosis
Benign cephalic histiocytosis (also known as Histiocytosis with intracytoplasmic worm-like bodies and not to be confused with Neonatal cephalic pustulosis) is a rare cutaneous condition affecting boys and girls equally […]