Cervical cystic lymphangioma in an adult: a rare entity

Authors

  • Jayesh Patel Department of Vascular Surgery, Shree Krishna Hospital and Pramukh Swami Medical College, Bhaikaka University, Gokalnagar, Karamsad, Anand, Gujarat, India https://orcid.org/0000-0001-5264-3698
  • Haryax Pathak Department of General Surgery, Shree Krishna Hospital and Pramukh Swami Medical College, Bhaikaka University, Gokalnagar, Karamsad, Anand, Gujarat, India https://orcid.org/0000-0003-3683-3672
  • Parth Baldaniya Department of General Surgery, Shree Krishna Hospital and Pramukh Swami Medical College, Bhaikaka University, Gokalnagar, Karamsad, Anand, Gujarat, India
  • Parth Ladani Department of General Surgery, Shree Krishna Hospital and Pramukh Swami Medical College, Bhaikaka University, Gokalnagar, Karamsad, Anand, Gujarat, India

DOI:

https://doi.org/10.18203/2349-2902.isj20243571

Keywords:

Cystic lymphangioma, Lymphangioma, Cystic hygroma, Cavernous lymphangioma, Lymphatics, Lymphatic malformation

Abstract

Lymphangiomas are benign malformations of the lymphatic system, commonly arising from sequestered lymphatic vessels. While typically found in infancy or childhood, their occurrence in adults is rare. This case details a 44-year-old female with a progressively enlarging, painless neck mass. Imaging revealed a cystic lesion near major neck vessels. Fine-needle aspiration cytology initially suggested lymphocele, while ultrasonography and computed tomography angiography provided differential diagnoses, including lymphangioma. Surgical excision of the mass and histopathological examination confirmed the diagnosis of cavernous lymphangioma. Although benign, lymphangiomas can cause complications through invasion of surrounding structures, leading to mass effects or secondary infections. Definitive management is surgical excision, but thorough imaging and differential diagnosis are critical to ruling out other potential conditions, especially given the rarity of lymphangiomas in adulthood.

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Published

2024-11-27

Issue

Section

Case Reports