Langerhans Cell Histiocytosis of the Right Scapula | Zendy

Maryam Moradi | Zendy; Sepideh Babaniamansour | Zendy; M Majidi | Zendy; Sepideh Karkon Shayan | Zendy; MD Firouzabadi | Zendy; Ahmadreza Atarodi | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Open Access

Langerhans Cell Histiocytosis of the Right Scapula

Author(s) -

Maryam Moradi,

Sepideh Babaniamansour,

M Majidi,

Sepideh Karkon Shayan,

MD Firouzabadi,

Ahmadreza Atarodi

Publication year - 2021

Publication title -

journal of biomedical research and environmental sciences

Language(s) - English

Resource type - Journals

ISSN - 2766-2276

DOI - 10.37871/jbres1223

Subject(s) - langerhans cell histiocytosis , scapula , medicine , histiocytosis , lesion , pathology , rare disease , lytic cycle , disease , anatomy , immunology , virus

Langerhans Cell Histiocytosis (LCH) is a rare granulomatous disease with an unknown origin. LCH occurs at any age and affects any organ. It is presented as self-limited to aggressive forms. Late diagnosis of LCH, after the evidence is revealed at the radiological imaging or microscopic investigations, aggravates the possible complications. This study reported a rare case of LCH with a bone lytic lesion at the right scapula with a good prognosis.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.

Having issues? You can contact us here

Accelerating Research