Spindle Cell Lipoma: Review of the Literature and Report of First Case in the Nasopharynx

2004 ◽  
Vol 131 (2) ◽  
pp. P306-P306
Author(s):  
Keith Arthur Swartz ◽  
Mark E Boseley
Author(s):  
Shaghauyegh S. Azar ◽  
Floyd Buen ◽  
Jennifer J. Chia ◽  
Yue Ma ◽  
Justin Caron ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-3
Author(s):  
Alberto Peña-Valenzuela ◽  
Nathalia García León

Spindle cell lipoma of the hypopharynx is an extremely rare entity. Here, we present the first case of this lesion originated in the cricopharyngeal region, with symptoms of chronic progressive dysphagia, which can be confused with other pathologies; endoscopic and magnetic resonance imaging (MRI) evaluation are the methods of choice for its diagnostic approach. The best therapeutic approach is endoscopic resection with rapid recovery and few complications. Long-term followup is recommended, either endoscopic or imaging, given that it can be confused with an undiagnosed liposarcoma; additionally, its long-term behavior is unknown.


2016 ◽  
Vol 2016 ◽  
pp. 1-4
Author(s):  
Abdulrahim AlAbdulsalam ◽  
Maha Arafah

Dendritic fibromyxolipoma is a rare and distinctive soft tissue neoplasm that is considered by many authors as a variant of spindle cell lipoma and characterized by the presence of dendritic cytoplasmic processes, plexiform vascular pattern, and keloidal collagen. It has never been reported in the larynx and hypopharynx. Its rarity and the potential to mistake it as a more clinically aggressive myxoid soft tissue neoplasm highlight the importance of its recognition. Here, a case of a dendritic fibromyxolipoma of the pyriform sinus in a 38-year-old male who presented with dysphagia, change of voice, and stridor is reported. A review of the literature, including histopathologic features and differential diagnosis, is also included.


2021 ◽  
Vol 64 (3) ◽  
pp. 174-182
Author(s):  
Manveen Kaur Jawanda ◽  
Harshaminder Kaur Grewal ◽  
Sonia Gupta ◽  
Vineet Sharma ◽  
Ravi Narula

Spindle cell lipoma (SCL) is an uncommon histological variant of lipoma that accounts for 1.5% of all adipose tumors. It rarely occurs in the oral cavity. The most common sites of involvement are the buccal mucosa, tongue, lip, alveolar mucosa, gingiva, and palate. Submandibular space is a very rare site of occurrence for SCL. When occurs in this site, SCL mainly involves the 4th–7th decade with a female predominance. Due to wide communications of submandibular space, the actual extent and appearance of the lesions present here gets masked up especially those involving the deeper tissues leading to an inaccurate diagnosis. Wide overlap of clinical and histopathological features of SCL to other clinical pathologies leads to a challenging task for the clinicians to reach an accurate diagnosis. To our knowledge, only four cases of intraoral SCL involving the submandibular region directly or indirectly have been reported in the literature. Here we represent another rare case of SCL in an 18-year-old male patient along with a concise review of the literature. This case appears to be quite rare due to its location (submandibular space), age, and sex of the patient (18/M).


2001 ◽  
Vol 51 (4) ◽  
pp. 301-304 ◽  
Author(s):  
Keisuke Horiuchi ◽  
Hiroo Yabe ◽  
Kazumasa Nishimoto ◽  
Noriko Nakamura ◽  
Yoshiaki Toyama

2015 ◽  
Vol 1 (1) ◽  
pp. 12-14 ◽  
Author(s):  
Michael Miloro ◽  
Anastasia Haupt ◽  
Alexis B. Olsson ◽  
Antonia Kolokythas

2011 ◽  
Vol 15 (5) ◽  
pp. 502-506 ◽  
Author(s):  
Damien Petit ◽  
Philippe Menei ◽  
Henri-Dominique Fournier

The authors describe the first case of spindle cell lipoma of the posterior neck invading the upper cervical spinal canal and the posterior cranial fossa. Spindle cell lipoma is an extremely rare variant of benign lipoma. It usually occurs as a solitary subcutaneous well-circumscribed lesion in the posterior neck or shoulders of adult men. Local aggressiveness is unusual. This 61-year-old man presented with an increased left cerebellar syndrome and headaches. He also had a posterior neck tumefaction, which had been known about for a long time. Computed tomography and MR imaging studies revealed a voluminous mass extending to the upper cervical canal and posterior cranial fossa and eroding the neighboring bones. The lesion was well delimited, and contrast enhancement was intense and heterogeneous. The tumor, which had initially developed under the muscles of the posterior neck, was totally resected. Histological assessment revealed numerous fat cells with spindle cells secreting collagen. The large size of the tumor and the submuscular location, bone erosion, and compression of the CNS were unusual in this rare subtype of benign adipose tumor. Its presentation could simulate a sarcoma.


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