“…However, the first case was reported by Sabouraud [2] in 1931 as "parakeratosamicrobienna du about des doigts." The term "parakeratosis pustulosa" was proposed by Hjorth and Thomsen [3] in Treatment depends on severity and includes topical (corticosteroids, vitamin D analogues, 5-fluorouracil, calcineurin inhibitors, retinoids), systemic (cyclosporine, methotrexate), and physical (phototherapy, photochemotherapy) therapies [10][11][12] Treatment depends on severity and includes topical (corticosteroids, retinoids), systemic (cyclosporine, methotrexate, acitretin, apremilast, biologic therapies), and physical (phototherapy) therapies [13] Systemic antibiotics may be combined with surgical drainage [14] Skin Appendage Disord 2022;8:435-440 DOI: 10.1159/000522671 1967, while reviewing such cases. Hence, the disease is also known as Hjorth-Sabouraud disease.…”