Papular nevus spilus syndrome: a further three cases
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sclosures. Financial support: none. Conflicts of interest: none.
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1 Unit of Dermatology, Department of Medicine (DIMED), University of Padua, via Vincenzo Gallucci 4, 35128, Padova Italy 2 Unit of Kidney and Pancreas Transplantation, Department of Surgical, Oncological and Gastroenterological Sciences, University of Padua, via Giustiniani 2, 35128, Padova Italy
a Theses
Emma SARTOR1,a Alvise SERNICOLA1,a Cristina SILVESTRE2 Flavia NERI2 Mauro ALAIBAC1
authors contributed equally
1. Ba˘ gci IS, Horváth ON, Ruzicka T, Sárdy M. Bullous pemphigoid. Autoimmun Rev 2017; 16: 445-55. 2. Heymann WR. Bullae for you: the increasing importance and implications of drug-induced bullous pemphigoid. J Am Acad Dermatol 2018; 79: 1026-7. 3. Weissenbacher A, Hautz T, Zelger B, et al. Bullous pemphigoid eleven years after bilateral hand transplantation. Am J Transplant 2012; 12: 1064-5. 4. Bhowmik DM, Dinda AK, Mahanta P, Agarwal SK. The evolution of the Banff classification schema for diagnosing renal allograft rejection and its implications for clinicians. Indian J Nephrol 2010; 20: 2-8. 5. Abdul Salim S, Thomas L, Quorles A, Hamrahian SM, Fülöp T. New diagnosis of bullous pemphigoid after withdrawal of immunosuppressive therapy in a failed renal transplant recipient on hemodialysis. Hemodial Int 2018; 22: E26-32. 6. Davenport A, Verbov JL, Golddsmith HJ. Circulating anti-skin basement membrane zone antibodies in a patient with Goodpasture’s syndrome. Br J Dermatol 1987; 117: 125-7. 7. Koratala A, Clapp WL, Olaoye OA, Santos AH. The skinkidney connection: bullous pemphigoid associated with acute allograft rejection and membranous nephropathy. Clin Case Reports 2018; 6: 432-3. 8. Stavropoulos PG, Soura E, Antoniou C. Drug-induced pemphigoid: a review of the literature. J Eur Acad Dermatol Venereol 2014; 28: 1133-40. 9. Sofi AA, Gottwald L, Bohman K, Kaw D. Bullous pemphigoid associated with acute renal allograft rejection. Transplantation 2010; 89: 368-9. doi:10.1684/ejd.2020.3837
Papular nevus spilus syndrome: a further three cases In 2019, we published a reappraisal and review paper on papular nevus spilus (PNS) syndrome. At that time, we had gathered 20 well defined cases of this condition [1]. Since then, we have identified two additional (previously overlooked) cases in the literature which were not covered by major biomedical search engines [2, 3]. Further reconsideration prompted us to also include an additional, previously reported case [4]. Considering the extreme rarity of PNS syndrome, we believe it appropriate to report the main features of these cases for the purpose of completeness and benefit of future research on the topic. These additional data confirm and further strengthen the findings and conclusions of our previous study [1], and increase the total number of known PNS syndrome cases to 23 (table 1).
EJD, vol. 30, n◦ 4, July-August 2020
EJD, vol. 30, n◦ 4, July-August 2020
443
48
11
27
23
29*
30*
2*
6*
15
41
43
30
42
-
3*
7*
4*
5*
11*
4
31
44
18
28*
*
59
27*
-
Male
Male
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