L90.2

Clinical Causes: Previous skin infections or inflammatory skin diseases Scarring from conditions like tuberculosis or leprosy Presence of autoimmune disorders such as lupus erythematosus Secondary to skin trauma or injury Rarely, associated with systemic illnesses like systemic sclerosis

Key Symptoms: Localized, soft, or pouch-like skin lesions Patches with a wrinkled or rippled appearance Areas of relative skin laxity that may feel wrinkled upon pinching Lesions typically asymptomatic but may occasionally cause mild discomfort Lesions tend to be stable over time without significant changes in size or shape Commonly found on the trunk, chest, or limbs

Diagnosis Path: Diagnosis of anetoderma of Jadassohn-Pellizzari involves a combination of clinical evaluation and skin biopsies. Healthcare providers look for characteristic stretchable, slack skin patches that stand out from surrounding areas. A skin biopsy often reveals a localized loss of elastic fibers within the dermis, confirmed through special staining techniques such as Verhoeff-Van Gieson. Additional tests may be conducted to exclude underlying systemic conditions or associated diseases, depending on the clinical scenario.

Treatment Protocols: There is currently no definitive cure for anetoderma. Management focuses on monitoring the lesions and addressing any underlying conditions, if identified. Cosmetic procedures, such as surgical excision or laser treatments, have been attempted to improve appearance but are not universally effective. Preventive measures include avoiding skin trauma and inflammatory triggers when possible. Patients are advised to consult with dermatologists for tailored management options and supportive care.