Reticulohistiocytosis

From WikiMD.org
Jump to navigation Jump to search

Reticulohistiocytosis

Reticulohistiocytosis (pronunciation: re-tic-u-lo-his-ti-o-cy-to-sis) is a rare disorder characterized by the accumulation of histiocytes, a type of immune cell, in the skin and other organs.

Etymology

The term "Reticulohistiocytosis" is derived from the Latin words 'reticulum' meaning 'net', 'histio' meaning 'tissue', and 'cytosis' meaning 'condition of cells'.

Definition

Reticulohistiocytosis is a rare non-Langerhans cell histiocytosis characterized by the accumulation of histiocytes in the skin and other organs. The disease can present in a variety of forms, including solitary cutaneous reticulohistiocytosis, multicentric reticulohistiocytosis, and diffuse cutaneous reticulohistiocytosis.

Symptoms

Symptoms of reticulohistiocytosis can vary widely, but often include skin lesions, joint pain, and in severe cases, organ dysfunction.

Diagnosis

Diagnosis of reticulohistiocytosis typically involves a combination of physical examination, medical history, and laboratory tests. A biopsy of affected tissue may also be performed to confirm the diagnosis.

Treatment

Treatment for reticulohistiocytosis is typically aimed at managing symptoms and may include medications to reduce inflammation and slow the progression of the disease. In severe cases, surgery may be required to remove large or problematic lesions.

Related Terms

External links

Esculaap.svg

This WikiMD article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski