Introduction: Pediatric eyelid masses pose a diagnostic challenge, with overlapping presentations between infectious, inflammatory, and neoplastic etiologies. Subcutaneous pyogenic granulomas (SPG), a rare variant, can mimic malignant tumors such as soft tissue sarcomas, leading to potential delays in appropriate management. This case report details the surgical resection of a rapidly growing pediatric eyelid subcutaneous mass, ultimately diagnosed as a subcutaneous pyogenic granuloma with histologic variation.
Methods: A 4-year-old male presented with a rapidly growing left upper eyelid mass. Ophthalmologic evaluation, ultrasonography, and orbital MRI with contrast were performed, revealing a highly vascular lesion. Due to rapid growth and concern for malignancy, the patient underwent a surgical biopsy with a frozen section, followed by complete excision. Intraoperative dissection was performed carefully to preserve surrounding eyelid structures.
Results: The excised mass measured ~2×3 cm and was highly vascular. Histopathology revealed anastomosing capillary nodules with mild mitotic activity and minimal atypia, consistent with SPG. At postoperative day 37, the patient showed no signs of recurrence.
Conclusions: Accurate diagnosis of pediatric eyelid masses is essential to guide treatment and avoid unnecessary morbidity. When clinical and imaging findings are inconclusive, surgical excision with histopathologic examination remains the gold standard. This case highlights the importance of a broad differential and multidisciplinary approach in managing pediatric eyelid lesions.
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http://dx.doi.org/10.1097/SCS.0000000000011205 | DOI Listing |
Surv Ophthalmol
March 2025
Tecnologico de Monterrey, School of Medicine and Health Sciences, Institute of Ophthalmology and Visual Sciences, Pediatric Ophthalmology and Strabismus Service, Monterrey, Mexico.
Exposure keratopathy (EK) is an underestimated ocular surface disorder that involves multiple underlying pathophysiologic mechanisms. It results from an exposed cornea due to different causes of eyelid insufficiency or blinking dysfunction, ocular globe protrusion, a negative orbital vector, and diverse contributing factors leading to impaired ocular surface homeostasis and the potential for vision loss. EK can be congenital, acquired, or induced, and various risk factors predispose patients to exposure to keratopathy.
View Article and Find Full Text PDFJ Craniofac Surg
March 2025
Department of Surgery, Division of Plastic Surgery, Nemours Children's Hospital Wilmington, DE.
Introduction: Pediatric eyelid masses pose a diagnostic challenge, with overlapping presentations between infectious, inflammatory, and neoplastic etiologies. Subcutaneous pyogenic granulomas (SPG), a rare variant, can mimic malignant tumors such as soft tissue sarcomas, leading to potential delays in appropriate management. This case report details the surgical resection of a rapidly growing pediatric eyelid subcutaneous mass, ultimately diagnosed as a subcutaneous pyogenic granuloma with histologic variation.
View Article and Find Full Text PDFBMC Ophthalmol
March 2025
Department of Ophthalmology, Seoul National University College of Medicine, Seoul, Korea.
Background: To investigate the morphological and functional changes of meibomian glands (MG) in pediatric patients who underwent surgery for lower eyelid epiblepharon.
Methods: A total of 176 eyes of 88 patients aged 19 and under (mean age: 8.9 ± 2.
J Med Case Rep
March 2025
Department of Ophthalmology, Osaka Medical and Pharmaceutical University, 2-7 Daigaku-machi, Takatsuki, Osaka, 569-8686, Japan.
Background: To date, there have been few detailed reports of the clinical findings in cases of fungal blepharitis. In this report, we present a rare case of anterior blepharitis in a Japanese child in whom Candida albicans was identified from secretions on the eyelash roots and present the clinical findings of the patient's eyelid margin via photograph documentation.
Case Presentation: This study involved a 6-year-old Japanese boy with Treacher-Collins syndrome and severe ulcerative colitis who, during a follow-up visit at the Department of Pediatrics at Osaka Medical and Pharmaceutical University Hospital, Takatsuki City, Osaka, Japan, suffered a cardiac arrest due to massive gastrointestinal hemorrhage, which led to persistent altered consciousness following resuscitation.
Am J Med Genet A
March 2025
Genetic Health Western Australia, Subiaco, Australia.
Blepharocheilodontic syndrome (BCD syndrome) is an autosomal dominant condition characterized by cleft lip/palate, distinct eyelid abnormalities, and ectodermal changes affecting hair and teeth. This report presents a novel case of CTNND1-related BCD syndrome in a 3-year-old female. In addition to the typical features, including unilateral cleft lip/palate and eyelid malformations, the patient exhibited a duplex kidney, ureterocele, and a bicornuate uterus-phenotypic traits not previously associated with BCD syndrome.
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