Orbital Lipofibromatosis in a Pediatric Patient.


Journal

Ophthalmic plastic and reconstructive surgery
ISSN: 1537-2677
Titre abrégé: Ophthalmic Plast Reconstr Surg
Pays: United States
ID NLM: 8508431

Informations de publication

Date de publication:
Historique:
pubmed: 17 7 2021
medline: 16 11 2021
entrez: 16 7 2021
Statut: ppublish

Résumé

A 10-month-old boy presented with a 3-month history of progressive left lower eyelid swelling. Examination demonstrated left lower eyelid fullness and hyperglobus with a fatty appearing inferior fornix mass. Imaging showed a mass isointense to fat in the left lower eyelid extending posteriorly, surrounding the inferior oblique with complete fatty infiltration, obscuration of the inferior rectus, and adherence to the globe. The patient underwent orbitotomy with biopsy and debulking of the tumor. Surgical pathology showed multiple fragments of adipose tissue with foci of plump and spindle-shaped cells arranged in bundles and fascicles, consistent with lipofibromatosis. This case illustrates a rare presentation of orbital lipofibromatosis in a pediatric patient.

Identifiants

pubmed: 34269771
doi: 10.1097/IOP.0000000000002008
pii: 00002341-202111000-00024
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202-e204

Informations de copyright

Copyright © 2021 The American Society of Ophthalmic Plastic and Reconstructive Surgery, Inc.

Déclaration de conflit d'intérêts

The authors have no financial or conflicts of interest to disclose.

Références

Fetsch JF, Miettinen M, Laskin WB, et al. A clinicopathologic study of 45 pediatric soft tissue tumors with an admixture of adipose tissue and fibroblastic elements, and a proposal for classification as lipofibromatosis. Am J Surg Pathol. 2000;24:1491–1500.
Boos MD, Chikwava KR, Dormans JP, et al. Lipofibromatosis: an institutional and literature review of an uncommon entity. Pediatr Dermatol. 2014;31:298–304.
Herrmann BW, Dehner LP, Forsen JW Jr. Lipofibromatosis presenting as a pediatric neck mass. Int J Pediatr Otorhinolaryngol. 2004;68:1545–1549.
Nuruddin M, Osmani M, Mudhar HS, et al. Orbital lipofibromatosis in a child: a case report. Orbit. 2010;29:360–362.
Taran K, Woszczyk M, Kobos J. Lipofibromatosis presenting as a neck mass in eight-years old boy–a case report. Pol J Pathol. 2008;59:217–220.
Kabasawa Y, Katsube K, Harada H, et al. A male infant case of lipofibromatosis in the submental region exhibited the expression of the connective tissue growth factor. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007;103:677–682.
Al-Ibraheemi A, Folpe AL, Perez-Atayde AR, et al. Aberrant receptor tyrosine kinase signaling in lipofibromatosis: a clinicopathological and molecular genetic study of 20 cases. Mod Pathol. 2019;32:423–434.
Vogel D, Righi A, Kreshak J, et al. Lipofibromatosis: magnetic resonance imaging features and pathological correlation in three cases. Skeletal Radiol. 2014;43:633–639.
Kenney B, Richkind KE, Friedlaender G, et al. Chromosomal rearrangements in lipofibromatosis. Cancer Genet Cytogenet. 2007;179:136–139.
Saab ST, McClain CM, Coffin CM. Fibrous hamartoma of infancy: a clinicopathologic analysis of 60 cases. Am J Surg Pathol. 2014;38:394–401.
Dutton JJ, Escaravage GK Jr, Fowler AM, et al. Lipoblastomatosis: case report and review of the literature. Ophthalmic Plast Reconstr Surg. 2011;27:417–421.
Kim OH, Kim YM. Calcifying aponeurotic fibroma: case report with radiographic and MR features. Korean J Radiol. 2014;15:134–139.

Auteurs

Angela Y Chang (AY)

Edward S. Harkness Eye Institute, Department of Ophthalmology, Columbia University Irving Medical Center-New York-Presbyterian Hospital, New York, New York, U.S.A.

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