Solitary fibrous tumor of the hypopharynx: Case report and literature review




Abstract


Solitary fibrous tumors are rare mesenchymal neoplasms that are increasingly being described in the head and neck. Clinical presentations may include compression by these tumors on vital surrounding structures. While malignant transformation is rare, treatment entails wide local excision. We present the case of a 74 year-old female with an increasingly enlarging symptomatic hypopharyngeal solitary fibrous tumor that was found on carotid duplex ultrasound. Transoral surgical excision resulted in relief of symptoms. Treatment options are discussed and a literature review of this uncommon disorder presented.



Introduction


Solitary fibrous tumor (SFT) is an uncommon, slow-growing, mesenchymal neoplasm that was initially described in 1931 arising from the pleura . Since this first case, SFTs have been described in the abdominal cavity, extremities, retroperitoneum, and head and neck region . The first reported case in the upper aerodigestive tract was in 1991, and there are less than 200 reported cases in the head and neck, with the most common sites being the oral cavity and paranasal sinuses . To our knowledge, we present the 3rd reported case of a SFT arising from the hypopharynx, with successful treatment using transoral surgery ( Table 1 ) .



Table 1

Hypopharyngeal solitary fibrous tumors reported in the literature.




























Study Tumor Size (cm) Presenting Symptoms Surgical Approach Disease-free follow-up (mo)
Mussak et al. 4.5 × 4 × 3.2 Progressive Dysphagia, 30 lb wt. loss Lateral pharyngotomy 18
Hanna et al. 4.1 × 3 × 1.2 Progressive Dysphagia Transoral 9
Present Study 4 × 2 × 2 Progressive dysphagia, dysphonia Transoral 9





Case report


A 74-year-old female with a one-year history of progressive dysphagia and dysphonia presented to our tertiary academic medical center with a hypopharyngeal mass. This mass was incidentally found on a carotid duplex ultrasound of the neck. An outside biopsy was inconclusive. An MRI was significant for a 4 × 2 × 2 cm hypopharyngeal mass compressing the airway medially and abutting the carotid artery laterally ( Fig. 1 ).




Fig. 1


Coronal T1-weighted MRI revealing a well-defined enhancing mass in the right hypopharynx.


She was then taken to the operating room and underwent microsuspension direct laryngoscopy and biopsy. Intraoperative frozen sections were nondiagnostic. Therefore, transoral CO2 laser debulking was undertaken. The tumor was densely adherent to the lateral hypopharyngeal wall. Final pathology revealed low grade spindle cell neoplasm consistent with SFT ( Figs. 2 and 3 ). Nine-months postoperatively, she is asymptomatic with no mucosal irregularities on flexible laryngoscopy. She has elected conservative management with close clinical and radiologic follow-up.




Fig. 2


Hematoxylin and eosin stain at high magnification (× 20) revealing small spindle shaped cells individually separated by thin bands of collagen fibers arranged haphazardly. Note the thin walled ectatic vessel in the center.

Aug 24, 2017 | Posted by in OTOLARYNGOLOGY | Comments Off on Solitary fibrous tumor of the hypopharynx: Case report and literature review

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