Disseminated superficial actinic porokeratosis (DSAP) L56.5 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM L56.5 became effective on October 1, 2018. This is the American ICD-10-CM version of L56.5 - other international versions of ICD-10 L56.5 may differ.
Clinical variants, which are most commonly seen in the pediatric population, include linear porokeratosis, porokeratosis of Mibelli, and porokeratosis palmaris et plantaris disseminata (also known as plantar porokeratosis).
The classic porokeratosis of Mibelli presents in infancy to early adulthood as an asymptomatic to slightly pruritic, brown to skin-colored, annular plaque with a peripheral hyperkeratotic, ridge-like scale. Lesions can range in size from 1 to 2 mm up to several centimeters in diameter.
Group of mostly hereditary disorders characterized by thickening of the palms and soles as a result of excessive keratin formation leading to hypertrophy of the stratum corneum (hyperkeratosis). ICD-10-CM L85.2 is grouped within Diagnostic Related Group (s) (MS-DRG v38.0): 606 Minor skin disorders with mcc 607 Minor skin disorders without mcc
Porokeratosis of Mibelli is a skin condition that usually develops in children or young adults. It begins as one or a few small, brownish bumps that grow into raised, bumpy patches. These patches slowly increase in size over time.
ICD-10-CM Code for Disseminated superficial actinic porokeratosis (DSAP) L56. 5.
Porokeratosis is a clonal disorder of keratinization characterized by one or more atrophic patches surrounded by a clinically and histologically distinctive hyperkeratotic ridgelike border called the cornoid lamella.
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The ICD-10-CM code that was billed was B35. 1 (Onychomycosis).
Summary. Disseminated superficial actinic porokeratosis (DSAP) is a skin condition that causes dry, scaly patches. Symptoms include a large number of small, brownish patches with a distinctive border, found most commonly on sun-exposed areas of the skin (particularly the lower arms and legs).
Porokeratosis is a skin condition which appears as raised brown bumps that may expand into scaly patches. They often have raised rings around the spots.
Porokeratosis is a rare, acquired or inherited disorder of keratinization characterized by one or more atrophic macules or patches, each surrounded by a distinctive hyperkeratotic, ridge-like border called "cornoid lamella" (picture 1D) [1,2]. Multiple clinical variants of porokeratosis exist.
buttocksThere are several names for this area: natal cleft, gluteal crease, gluteal crevice. This area is the groove between the buttocks that extends from just below the sacrum to the perineum, above the anus and is formed by the borders of the large buttock muscles called the gluteus maximus.
Pressure ulcer of unspecified buttock, unspecified stage The 2022 edition of ICD-10-CM L89. 309 became effective on October 1, 2021.
ICD-10-CM Code for Disorder of the skin and subcutaneous tissue, unspecified L98. 9.
Lesions can range in size from 1 to 2 mm up to several centimeters in diameter.
Porokeratosis is a disorder of keratinization characterized by hyperkeratotic papules or plaques surrounded by a distinct peripheral, thin, ridge-like scale that expands centrifugally. Several variants of porokeratosis have been described, and a wide overlap between variants exists, suggesting that they are close in relation. Clinical variants, which are most commonly seen in the pediatric population, include linear porokeratosis, porokeratosis of Mibelli, and porokeratosis palmaris et plantaris disseminata (also known as plantar porokeratosis). Porokeratosis ptychotropica is a rare variant that presents in adults in the intergluteal cleft and extending onto the buttocks. All variants share a distinctive histological feature known as the cornoid lamella, which corresponds to the hyperkeratotic ridge surrounding these lesions.
Lesions can range in size from 1 to 2 mm up to several centimeters in diameter . Larger lesions tend to form on the lower leg and foot, although giant facial and genital lesions have been described. The condition may be inherited as an autosomal dominant trait. Antecedent trauma or immunosuppression may be present.
Porokeratosis Ptychotropica. Porokeratosis ptychotropica is a rare variant that has been reported in adults. Most reported cases have been in males. Giant plaques with a verrucous surface may be seen on the buttocks. It has been reported to coexist with porokeratosis of Mibelli.