Abstract: Facial Infiltrating Lipomatosis Contains Somatic PIK3CA Mutations in Multiple Tissues (Plastic Surgery 2015)

Saturday, October 17, 2015: 2:10 PM

Javier A Couto, BS , Plastic Surgery, Boston Children's Hospital / Harvard Medical School, Boston, MA

Matthew P Vivero, BA , Plastic Surgery, Boston Children's Hospital / Harvard Medical School, Boston, MA

Joseph Upton, MD , Plastic & Oral Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA

Bonnie L Padwa, DMD, MD , Plastic & Oral Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA

Matthew L Warman, MD , Orthopaedic Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA

John B Mulliken, MD , Plastic Surgery, Boston Children's Hospital, Harvard Medical School, Boston, MA

Arin K Greene, MD, MMSc , Plastic Surgery, Boston Children's Hospital / Harvard Medical School, Boston, MA

Presentation PDF file

BACKGROUND: Facial infiltrating lipomatosis (FIL) is a rare congenital disorder that causes overgrowth of one side of the face, that can include premature dental eruption, hemimacroglossia, macrodontia, and mucosal neuromas. We recently reported that affected subcutaneous adipose tissue in patients with FIL contains mutant cells with somatic gain-of-function mutations in PIK3CA.¹ The purpose of this study was to determine whether other affected tissues in FIL also contain mutant cells.

METHODS: We obtained FIL tissue from 2 patients during a clinically-indicated procedure. We isolated skin, subcutaneous fat, muscle, buccal fat, and mucosal neuroma tissues, and cultured CD31⁺ endothelial cells. We then performed droplet digital PCR (ddPCR) on DNA from each tissue and the cultured endothelial cells to determine the frequencies of PIK3CA mutant alleles in the different tissues.

RESULTS: In one FIL specimen we identified a p.H1047R mutation that was present at allele frequencies of 5.5% in skin, 17.6% in subcutis, 23.2% in buccal fat, 12.5% in mucosal neuroma, and 1.2% in endothelial cells. In a second FIL specimen, we identified a p.H1047L mutation that was present at allele frequencies of 5.6% in muscle, 16.2% in subcutis, and 1.5% in endothelial cells (Figure).

CONCLUSIONS: Cells containing PIK3CA mutations are present in several different tissues that are affected in FIL. These data are consistent with the mutation arising in an early pluripotent cell gives rise to several different tissue types in the face, rather than the mutation arising in only one cell type and causing overgrowth of surrounding tissues via paracrine signaling.

FIGURE. (Left) Four-year-old male with facial infiltrating lipomatosis (FIL). (Right) Droplet digital (ddPCR) reaction showing PIK3CA mutation in muscle tissue from patient with FIL. Left upper quadrant represents droplets with only the mutant allele. Right upper quadrant shows droplets with mutant and wild-type alleles. Left lower quadrant represents droplets that do not contain any alleles. Right lower quadrant shows droplets with only the wild-type allele.

27923 Facial Infiltrating Lipomatosis Contains Somatic PIK3CA Mutations in Multiple Tissues