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Review Case Reports
Hypopharyngeal spindle cell lipoma: A case report and review of literature.
- Zheng Liang, Yiqing Zang, Zhibin Jing, Yujie Zhang, Hui Cao, and Huifang Zhou.
- Department of Otorhinolaryngology.
- Medicine (Baltimore). 2021 May 7; 100 (18): e25782e25782.
RationaleSpindle cell lipoma is a rare, uncommon type of benign lipomatous tumor, a distinct group of lipomas composed of mature adipocytes, uniform spindle cells, and multinucleated giant cells associated with ropey collagen. Immunohistochemically, spindle cell lipoma is characterized by the diffuse expression of CD34.Patient ConcernsWe present a rare case of a 56-year-old man who complained of vomiting out of a smooth and giant mass in the oral cavity provoked by an intra-abdominal pressure increase. Oral examination revealed an elongated mass protruding from the mouth. Computed tomography of the patient showed a mass from left pyriform to oral cavity, with 2.38 × 2.78 × 16.86 cm in size. The flexible fiberscope showed that the pedicle of the elongated mass originated from the posterior wall of the hypopharynx, corresponding to the left pyriform fossa.DiagnosisHistopathologically, the tumor was mainly composed of hyperplastic adipocytes, admixed with small blood vessels, and scattered inside adipose tissue spindle cells. The immunohistochemical profile revealed positivity of spindle cells for CD34, negativity for S100, and low proliferation with Ki67, which confirmed the diagnosis of spindle cell lipoma and revealed its benign behavior.InterventionsThe patient underwent hypopharyngeal mass resection using transoral suspension laryngoscopy.OutcomesNo recurrence was found after 5 months of follow-up.LessonsSpindle cell lipoma is difficult to diagnose early because of slow growth and subtle symptomatology. This entity should be differentiated from several benign or malignant subtypes of lipomas, including liposarcomas. In this case, the spindle cell lipoma is large and originates from the hypopharynx, which is a rare entity and presents with atypical symptoms. This case gave rise to further studies on the clinical and pathologic characteristics of this tumor in the future.Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
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