Syringocystadenocarcinoma Papilliferum in a Fifteen-Year-Old Girl: A Case Report and Review of the Literature

Author:

Halsey Jordan N.1ORCID,Faith Esteban Fernandez23ORCID,Logan Suzanna J.34ORCID,Shenoy Archana34ORCID,Schieffer Kathleen M.5ORCID,Cottrell Catherine E.35ORCID,Lillis Anna P.6ORCID,Aldrink Jennifer H.37ORCID,Setty Bhuvana A.8ORCID,Pearson Gregory D.13ORCID

Affiliation:

1. Department of Plastic Surgery, Nationwide Children’s Hospital, Columbus, OH, USA

2. Division of Dermatology, Department of Pediatrics, Nationwide Children’s Hospital, Columbus, OH, USA

3. The Ohio State University College of Medicine, Columbus, OH, USA

4. Department of Pathology and Laboratory Medicine, Nationwide Children’s Hospital, Columbus, OH, USA

5. The Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children’s Hospital, Columbus, OH, USA

6. Department of Radiology, Nationwide Children’s Hospital, Columbus, OH, USA

7. Department of Surgery, Division of Pediatric Surgery, Nationwide Children’s Hospital, Columbus, OH, USA

8. Division of Hematology/Oncology/BMT, Nationwide Children’s Hospital, Columbus, OH, USA

Abstract

Syringocystadenocarcinoma papilliferum (SCACP) is a rare malignant neoplasm arising from adnexal tissues and is the malignant complement to the benign neoplasm syringocystadenoma papilliferum (SCAP). SCACP lesions appear as raised nodules or inflammatory plaques and can be associated with SCAP or nevus sebaceous. There have been fewer than 100 described cases of this neoplasm in the literature, and all previously published cases have been described in adults, with the majority occurring in the elderly. We present a case of an adolescent female with a syringocystadenocarcinoma papilliferum arising from a large thigh mass harboring an in-frame alteration in MAP2K1 along with a brief review of the literature.

Publisher

Hindawi Limited

Subject

Dermatology

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