Idiopathic Cervical Lymphocele Mimicking Congenital Lymphatic Malformation

Lymphoceles are collections of lymphatic fluid that typically arise following surgical disruption of lymphatic channels, most commonly in the retroperitoneal or pelvic regions. Idiopathic presentations, especially in the cervical region, are extremely rare and may mimic congenital lymphatic malformations such as cystic hygroma and lymphangioma, complicating diagnosis. We present the case of a 30-year-old male with a neck mass that has been getting larger gradually and has caused no pain; it was associated with no previous trauma or surgery or history of infection. Imaging revealed a well-circumscribed, fluid-filled lesion that compressed adjacent cervical structures. Ultrasound-guided aspiration yielded clear lymphocyte-rich fluid, confirming the diagnosis of a lymphocele. The patient was successfully managed with bleomycin-based sclerotherapy, achieving complete resolution without recurrence over a five-year follow-up. This case emphasizes the importance of a comprehensive diagnostic approach, including clinical history, imaging, and cytological evaluation, to differentiate idiopathic lymphoceles from congenital lymphatic anomalies and highlights the efficacy of sclerotherapy as a minimally invasive therapeutic option.

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Publication Details

Journal
Cureus
Published
2025-12-22
DOI
https://doi.org/10.7759/cureus.99824
Primary Topic
Lymphatic Disorders and Treatments
Type
article
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article

Idiopathic Cervical Lymphocele Mimicking Congenital Lymphatic Malformation

Meher Jehan, Maaz Hamid, Muhammad Abdullah, Sabeeh Zahra
Cureus
Lymphatic Disorders and Treatments
article

Idiopathic Cervical Lymphocele Mimicking Congenital Lymphatic Malformation

Meher Jehan, Maaz Hamid, Muhammad Abdullah, Sabeeh Zahra
article en

Abstract

Lymphoceles are collections of lymphatic fluid that typically arise following surgical disruption of lymphatic channels, most commonly in the retroperitoneal or pelvic regions. Idiopathic presentations, especially in the cervical region, are extremely rare and may mimic congenital lymphatic malformations such as cystic hygroma and lymphangioma, complicating diagnosis. We present the case of a 30-year-old male with a neck mass that has been getting larger gradually and has caused no pain; it was associated with no previous trauma or surgery or history of infection. Imaging revealed a well-circumscribed, fluid-filled lesion that compressed adjacent cervical structures. Ultrasound-guided aspiration yielded clear lymphocyte-rich fluid, confirming the diagnosis of a lymphocele. The patient was successfully managed with bleomycin-based sclerotherapy, achieving complete resolution without recurrence over a five-year follow-up. This case emphasizes the importance of a comprehensive diagnostic approach, including clinical history, imaging, and cytological evaluation, to differentiate idiopathic lymphoceles from congenital lymphatic anomalies and highlights the efficacy of sclerotherapy as a minimally invasive therapeutic option.

CureusVol. 17(12)
Shifa Tameer-e-Millat University (PK), Shifa International Hospital (PK)
Good health and well-being
Openalex Percentile: Top 27%
Lymphatic Disorders and Treatments
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Idiopathic Cervical Lymphocele Mimicking Congenital Lymphatic Malformation — Meher Jehan, Maaz Hamid, et al. · Cureus (2025) | TGRS Research Map | TGRS