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A rare case of squamous inclusion cyst in cervical lymph node
Y Houcine1,2,3, A Sassi1,3, M Mlika1,2,3
1Pathology Department, Abderrahmen Mami Hospital, Ariana, Tunisia.
Insights
A rapidly enlarging squamous inclusion cyst in a jugular lymph node mimicked tuberculosis. This case highlights diagnostic challenges and the need to consider this rare lesion in cervical lymph node differentials.
Area of Science:
- Pathology
- Surgical Pathology
- Head and Neck Pathology
Background:
- Cervical lymphadenopathy is common, with tuberculosis and metastatic carcinoma being frequent considerations.
- Squamous inclusion cysts are benign lesions typically found in the skin, rarely presenting as rapidly enlarging lymph node masses.
- Distinguishing benign cysts from malignancy in lymph nodes poses a significant diagnostic challenge.
Observation:
- A 38-year-old man presented with a rapidly enlarging 2 cm jugular lymph node, initially suspected to be lymph node tuberculosis.
- Histopathological examination revealed a cystic structure lined by keratinizing squamous epithelium with a granular cell layer, consistent with a squamous inclusion cyst.
- Metastatic squamous cell carcinoma could not be definitively excluded based on initial findings.
Findings:
- This report details the first case of a rapidly enlarging squamous inclusion cyst within a jugular lymph node.
- The histological features mimicked malignancy, presenting a diagnostic dilemma.
- The lesion was confirmed as a squamous inclusion cyst, despite its unusual presentation and rapid growth.
Implications:
- This case underscores the importance of considering benign squamous inclusion cysts in the differential diagnosis of rapidly enlarging cervical lymphadenopathy.
- Awareness of this rare presentation can prevent misdiagnosis and unnecessary aggressive treatment.
- Further investigation into the pathogenesis of rapidly growing lymph node inclusion cysts may be warranted.
Abstract:
A 38-year-old man, with no history of malignancy, was found to have a 2 cm jugular lymph node, for which a lymph node tuberculosis was suspected. The specimen revealed a cystic structure lined by mature keratinizing squamous epithelium with a prominent granular cell layer consistent with a squamous inclusion cyst in a lymph node, but a metastatic squamous cell carcinoma could not be excluded. This is the first case report of a rapidly enlarging squamous inclusion cyst in a jugular lymph node. Our case demonstrates the diagnostic challenges related to a squamous inclusion cyst in cervical lymph node and serves to inform the readers to consider this lesion in the differential diagnosis for similar situations.

