TY - JOUR
T1 - Pterygium Inversum Unguis
T2 - Report of 19 Cases and Review of the Literature
AU - Caputo, Ruggero
AU - Cappio, Fiammetta
AU - Rigoni, Corinna
AU - Scarabelli, Gabriele
AU - Toffolo, Pietro
AU - Spinelli, Giuseppe
AU - Crosti, Carlo
PY - 1993
Y1 - 1993
N2 - Background: Pterygium inversum unguis is a rare abnormality of the nail bed that remains adherent to the ventral surface of the nail plate, resulting in a subungual extension of the hyponychium and obliteration of the distal groove. Objective: The aim of our article is to illustrate the cases of pterygium inversum unguis that we observed in the last 20 years and to discuss them according to a broad review of the literature. Results: Nineteen new cases of pterygium inversum unguis have been observed: one congenital idiopathic form, five acquired idiopathic forms, and 13 secondary forms. Conclusion: Our study and the review of the literature demonstrate that the most common forms of pterygium inversum unguis are the acquired secondary ones. They are generally related to systemic connective tissue diseases and, in particular, to progressive systemic sclerosis and systemic lupus erythematosus.
AB - Background: Pterygium inversum unguis is a rare abnormality of the nail bed that remains adherent to the ventral surface of the nail plate, resulting in a subungual extension of the hyponychium and obliteration of the distal groove. Objective: The aim of our article is to illustrate the cases of pterygium inversum unguis that we observed in the last 20 years and to discuss them according to a broad review of the literature. Results: Nineteen new cases of pterygium inversum unguis have been observed: one congenital idiopathic form, five acquired idiopathic forms, and 13 secondary forms. Conclusion: Our study and the review of the literature demonstrate that the most common forms of pterygium inversum unguis are the acquired secondary ones. They are generally related to systemic connective tissue diseases and, in particular, to progressive systemic sclerosis and systemic lupus erythematosus.
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U2 - 10.1001/archderm.1993.01680310077013
DO - 10.1001/archderm.1993.01680310077013
M3 - Article
C2 - 8215496
AN - SCOPUS:0027484573
SN - 0003-987X
VL - 129
SP - 1307
EP - 1309
JO - Archives of Dermatology
JF - Archives of Dermatology
IS - 10
ER -