scholarly journals Gastric Glomus Tumor: A Case Report

2021 ◽  
Vol 6 (2) ◽  
pp. 55-58
Author(s):  
Gio Earnest de la Cruz ◽  
◽  
Carolyn Marie Legaspi ◽  
Jose Carnate Jr.
Keyword(s):  
2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Ichiro Tamaki ◽  
Yohei Hosoda ◽  
Hironobu Sasano ◽  
Yu Sasaki ◽  
Hidenori Kiyochi ◽  
...  

Abstract Background Glomus tumors are subcutaneous tumors arising from glomus bodies, thermoregulatory components of the skin. These tumors could occur in visceral organs where glomus bodies are not normally present. Herein, we report a case of primary pancreatic glomus tumor with aggressive direct invasion into the superior mesenteric vein (SMV). To the best of our knowledge, this is the second case report of a glomus tumor arising in the pancreas. Case presentation A 46-year-old woman was referred to our hospital due to vomiting with epigastric and back pain. Dynamic-CT revealed a well-circumscribed hypervascular mass, measuring 37 mm in its maximal diameter involving the pancreatic head. Both CT and endoscopic ultrasonography (EUS) revealed direct invasion into the SMV and radiologically suspected tumor thrombus. Biopsy sample obtained by EUS-guided fine needle aspiration revealed proliferation of small cells, round-to-oval tumor cells with round nuclei and scant cytoplasm. A histological diagnosis of pancreatic neuroendocrine tumor, G1 was initially considered. Therefore, subtotal stomach-preserving pancreatoduodenectomy using Child-II reconstruction was subsequently performed. Her SMV was resected and reconstructed due to extensive tumor involvement. Subsequent histopathological analysis revealed solid tumor cells proliferation that comprised oval-shaped nuclei and scant cytoplasm around disorganized or slit-shaped vessels in hematoxylin–eosin-stained slides. Immunohistochemical analysis then demonstrated positive immunoreactivity for smooth muscle actin, vimentin, and CD34, but negative for chromogranin A, synaptophysin, CD56, and signal transducer and activator of transcription 6. Based on these histological findings of resected specimens, the lesion was subsequently diagnosed as a primary pancreatic glomus tumor harboring direct invasion into the SMV. Her postoperative course was uneventful and annual surveys for the following 4 years post-op detected no clinical signs of recurrence. Conclusions We report a very rare case of glomus tumor of the pancreas accompanied by venous invasion. Curative surgical resection is the best treatment option for pancreatic glomus tumors. Although pancreatic glomus tumor is rare, it should be taken into consideration in the differential diagnosis of a pancreatic solid tumor with hypervascularity.


2007 ◽  
Vol 96 (7) ◽  
pp. 633-636 ◽  
Author(s):  
Shigetoshi Matsuo ◽  
Seiya Susumu ◽  
Ryuji Tsutsumi ◽  
Takashi Azuma ◽  
Shirou Obata ◽  
...  
Keyword(s):  

2018 ◽  
Vol 12 (1) ◽  
Author(s):  
Ouiame EL Jouari ◽  
Salim Gallouj ◽  
Sara Elloudi ◽  
Ghita Senhaji ◽  
Mouna Rimani ◽  
...  
Keyword(s):  

2001 ◽  
Vol 27 (9) ◽  
pp. 837-840 ◽  
Author(s):  
John D. Kayal ◽  
Robin W. Hampton ◽  
Daniel J. Sheehan ◽  
Carl V. Washington

Author(s):  
Tajamul Rashid ◽  
Javed Altaf ◽  
Musharraf Husain ◽  
Shakil Jawed ◽  
Syed Salman

2018 ◽  
Vol 14 (1) ◽  
Author(s):  
Kazuto Kurohara ◽  
Yasuyuki Michi ◽  
Akane Yukimori ◽  
Satoshi Yamaguchi
Keyword(s):  

2020 ◽  
Vol 70 ◽  
pp. 197-200
Author(s):  
John G. Aversa ◽  
Cara Monroe ◽  
Amelia Levi ◽  
Antonios Papanicolau-Sengos ◽  
David E. Kleiner ◽  
...  
Keyword(s):  

2020 ◽  
Vol 25 (04) ◽  
pp. 508-512
Author(s):  
Jason D. Wink ◽  
Olatomide Familusi ◽  
Ines C. Lin

We present a case of a 26-year-old right hand dominant male landscaper with a slow growing right ring finger subungual mass. MRI confirmed a 0.9 × 1.5 × 0.9 cm well circumscribed subungual mass believed to be consistent with a glomus tumor, although size and symptoms were not consistent with that diagnosis. The mass was completely excised and diagnosis of schwannoma was confirmed by H&E histology. A literature search was performed utilizing the term “subungual schwannoma.” Four case reports were found describing this diagnosis in the hand as well as a single case report describing it in the foot. In summary, this is a 26-year-old male who presents with a schwannoma in the unusual subungual location. Although rare, based on our case and the existing literature, subungual schwannomas should be included in the differential diagnosis of a slow growing subungual mass, particularly if symptoms and exam are inconsistent with more common etiologies.


2020 ◽  
Vol 74 ◽  
pp. 232-234
Author(s):  
Philippe Drabent ◽  
Franck Bielle ◽  
Isabelle Bernat ◽  
Matthieu Peyre

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