| Literature DB >> 29595682 |
Kabalane Yammine1, Haydar A Nasser, Usama Hadi, Mohamad Ali Natout, Vicky Najjar, Claude Tayar.
Abstract
RATIONALE: Head and Neck Solitary fibrous tumors (SFT) are very rare. They could be misdiagnosed as hemangiopericytomas (HPC). PATIENT CONCERNS: We report a 60 y o lady presenting with sinonasal mass, causing recurrent profuse bleeding. DIAGNOSES: Hemangioperocytomas versus SFT were among the differentials, according to Radiological studies. Upon Biopsy, the diagnosis of SFT has been adopted.Entities:
Mesh:
Year: 2018 PMID: 29595682 PMCID: PMC5895367 DOI: 10.1097/MD.0000000000010251
Source DB: PubMed Journal: Medicine (Baltimore) ISSN: 0025-7974 Impact factor: 1.889
Figure 1Computed tomography (CT) scan showing a left nasal cavity mass extending to the maxillary sinus, pterygopalatine fossa, and infratemporal fossa (asterisk indicates tumor location in the frontal cut and a black arrow in the transverse cut).
Figure 2A, Pre-embolization angiography showing the vascular appearance of the tumor (white arrow). B, The micocatheter in the left internal maxillary artery (white arrowhead). C, Postembolization angiogram. “×” indicates the microcoil.
Figure 3A, Low power magnification of the tumor showing a densely cellular proliferation with numerous stellate and staghorn-like vessels (black arrow). The tumor shows no necrosis (H&E 50). B, Immunohistochemistry for CD34 is positive in the tumor cells (200) and around the staghorn vessel (double blue arrow).
Nasal and paranasal solitary fibrous tumors reported during the last 10 years.