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International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Hidradenitis suppurativa is a chronic disease characterised by recurrent, painful, deep-seated, rounded nodules and abscesses due to follicular occlusion with secondary inflammation and destruction of the pilo-sebaceo-apocrine apparatus and extension to the adjacent subcutaneous tissue. Subsequent hypertrophic scarring and suppuration of apocrine gland-bearing skin (axillae, groins, peri-anal and perineal regions) are the main clinical features. Infection and hormonal influence are described but are not the primary pathogenetic factor: the exact aetiology remains unknown. Obesity is common and is associated with more severe disease. The main complications are fistulae, arthropathy, carcinoma and amyloidosis.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Specific anatomy - multiple selections are allowed
synonyms
Hidradenitis suppurativa
Acne inversa
Inverse acne
Suppurative hidradenitis
Hidradenitis suppurativa of axillae
Acne inversa of axillae
Hidradenitis suppurativa of anogenital region
Acne inversa of anogenital region
Hidradenitis suppurativa affecting other specified sites