Lymphangiomas: Rare presentations in oral cavity and scrotum in pediatric age group

Ankush Arunrao Kurude1, Meghana Madhukar Phiske1, Ketan Kallapa Kolekar1

  • 1Department of Dermatology, Topiwala National Medical College and B.Y.L. Nair Ch. Hospital, Mumbai, Maharashtra, India.

Insights

Lymphangiomas, common in newborns, typically affect the head and neck. This study highlights rare cases of buccal and genital lymphangioma, emphasizing diverse clinical presentations and treatment considerations.

Area of Science:

  • Pediatric Surgery
  • Dermatology
  • Medical Genetics

Background:

  • Lymphangiomas are congenital benign tumors with an incidence of 1.2 to 2.8 per 1000 newborns.
  • They commonly present at birth or before two years of age, predominantly affecting the head and neck region (50%-70%).

Observation:

  • The buccal mucosa is the second most frequent site for lymphangioma, with 14 reported cases, following the anterior two-thirds of the tongue.
  • The scrotum is an exceptionally rare site, with fewer than 50 cases reported globally as of 2002.
  • This study details two rare cases: a primary, late-onset buccal lymphangioma with vesicular presentation and a genital lymphangioma involving the scrotum, thigh, and groin.

Findings:

  • The presented cases underscore the variability in lymphangioma presentation, including unusual locations and late-onset occurrences.
  • The management of lymphangioma often requires a multidisciplinary approach due to potential involvement of vital structures and functional/aesthetic concerns.

Implications:

  • Understanding the diverse clinical spectrum of lymphangioma is crucial for accurate diagnosis and timely intervention.
  • These rare case reports contribute to the existing literature, aiding clinicians in managing atypical lymphangioma presentations.
  • Further research into the etiology and optimal treatment strategies for rare lymphangioma variants is warranted.

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