Results 91 to 100 of about 146,388 (138)

Scaling red-brown hyperkeratotic papules and plaques involving the axilla

JAAD Case Reports
Michael C. Elias, BA, Christine C. Tam, MD   +1 more
doaj   +1 more source

Dermoscopic Characterization of Granular Parakeratosis: Toward a Recognizable Pattern

Dermatology Practical & Conceptual
Caterina Mariarosaria Giorgio, Michela Liguori, Mariachiara Arisi, Giuseppe Argenziano, Gaetano Licata   +4 more
doaj   +1 more source

Paraqueratosis granular intertriginosa

Intertriginous granular parakeratosis (IGP) was initially described as axillary granular parakeratosis. It is a rare, idiopathic, and self-limiting dermatosis.
Pérez Cáceres, Luis Daniel, Morales Cardona, Camilo Andrés   +1 more
core  

Infantile Granular Parakeratosis

The Journal of Pediatrics
Samantha Epstein, Sarah Williamson, Lisa Gelles   +2 more
openaire   +2 more sources

A 66‐Year‐old Woman With Submammary Brownish Hyperkeratotic Plaques

JEADV Clinical Practice
Antonia Kössinger, Michael Offers, Stephan Alexander Braun   +2 more
doaj   +1 more source

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Intertriginous granular parakeratosis

Journal of the American Academy of Dermatology, 1998
An unusual form of parakeratosis localized to the axillae has been previously described in the literature as axillary granular parakeratosis. We report an additional 4 cases, including one that was isolated to the inguinal region. The same histopathologic changes of papillomatosis, acanthosis, and parakeratosis with retention of keratohyalin granules ...
Darius R Mehregan
exaly   +3 more sources

Granular Parakeratosis in a Child

Pediatric Dermatology, 2002
Granular parakeratosis has only recently been described and typically occurs in adults. We report the first instance of this condition affecting a child.
Andrea B, Trowers, Rich, Assaf, Christine, Jaworsky   +2 more
exaly   +3 more sources

Granular parakeratosis: Pathologic and clinical correlation of 18 cases of granular parakeratosis

Journal of the American Academy of Dermatology, 2005
Granular parakeratosis (originally termed axillary granular parakeratosis) is an idiopathic, benign, nondisabling cutaneous disease that manifests with intertriginous erythematous, brown or red, scaly or keratotic papules and plaques. It presents in all age groups and has no established clinical associations.We wanted to assess the following: (1) the ...
Noah S Scheinfeld
exaly   +3 more sources

Granular parakeratosis: four paediatric cases

British Journal of Dermatology, 2002
Axillary granular parakeratosis (GP) was first described in 1991 as a peculiar eruption presenting with erythematous hyperpigmented and hyperkeratotic papules and plaques of the cutaneous folds frequently associated with pruritus. Histopathology shows a characteristic picture with a conspicuous granular appearance of the parakeratotic horny layer ...
Patrizi Annalisa, Iria Neri, P A Fanti
exaly   +3 more sources

Axillary granular parakeratosis: Response to isotretinoin

Journal of the American Academy of Dermatology, 1997
The term axillary granular parakeratosis has been proposed for a recently recognized eruption with distinct histopathologic features. In 1991 Northcutt, Nelson, and Tschen ~ described four patients with a well-demarcated axillary eruption that was clinically similar to Hailey-Hailey disease. Biopsy specimens, however, exhibited an unusual parakeratosis.
Kenneth S Resnik, Guy F Webster, G F Webster   +2 more
exaly   +3 more sources