giant neurofibroma
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Cureus ◽  
2021 ◽  
Author(s):  
Ioannis E Kougioumtzis ◽  
Antonia Barmpitsioti ◽  
Stylianos Tottas ◽  
Alexandra Giatromanolaki ◽  
Georgios I Drosos

2021 ◽  
Author(s):  
Samit Sharma ◽  
Biraj Pokhrel ◽  
Namrata Khadka ◽  
Sangam Rayamajhi ◽  
Jayan Man Shrestha ◽  
...  

2021 ◽  
Vol 104 (1) ◽  
pp. 003685042110042
Author(s):  
Haiying Zhou ◽  
Hui Lu

Neurofibroma is a rare nerve sheath tumor of neuroectodermal origin, especially the huge and isolated neurofibroma located in the inguinal region. To our knowledge, no such case has previously been reported. We report a case of 34-year-old male patient with a 4-year history of progressive enlargement of the medial root mass in his left thigh with sitting and standing disorders along with pain. The tumor was completely removed by operation, and pathological diagnosis showed neurofibroma. There was no obvious neurologic defect after surgery, and no recurrence tendency was found in the follow-up of 2 years. For a large solitary mass with slow growth and no malignant clinical manifestations for a long time, clinicians cannot rule out the hypothetical diagnosis of neurofibroma, even though its growth site is very rare, such as this case of a huge tumor located in the groin. For neurogenic tumors, early operation should be performed, and the prognosis of patients after tumor resection is excellent.


2020 ◽  
Vol 85 (4) ◽  
pp. 413-418
Author(s):  
Fei Liu ◽  
Feixue Din ◽  
Chuan Gu ◽  
Lin Lv ◽  
Xiuxia Wang ◽  
...  

2020 ◽  
Author(s):  
Haiying Zhou ◽  
Hui Lu

Abstract BackgroundNeurofibroma is a rare nerve sheath tumor of neuroectodermal origin, especially the huge and isolated neurofibroma located in the inguinal region. To our knowledge, no such case has previously been reported.Case presentationWe report a case of 34-year-old male patient with a 4-year history of progressive enlargement of the medial root mass in his left thigh with sitting and standing disorders along with pain. The tumor was completely removed by operation, and pathological diagnosis showed neurofibroma. There was no obvious neurologic defect after surgery, and no recurrence tendency was found in the follow-up of 2 years.ConclusionsFor a large solitary mass with slow growth and no malignant clinical manifestations for a long time, clinicians can not rule out the hypothetical diagnosis of neurofibroma, even though its growth site is very rare, such as this case of a huge tumor located in the groin. For neurogenic tumors, early operation should be performed, and the prognosis of patients after tumor resection is excellent.


2020 ◽  
Author(s):  
Haiying Zhou ◽  
Hui Lu

Abstract Background:Neurofibroma is a rare nerve sheath tumorofneuroectodermal origin, especially the huge and isolated neurofibroma located in the inguinal region. To our knowledge, no such case has previously been reported.Case presentation:We report a case of 34-year-old male patient with a 4-year history of progressive enlargement of the medial root mass in his left thigh with sitting and standing disorders along with pain. The tumor was completely removed by operation, and pathological diagnosisshowed neurofibroma. There was no obvious neurologic defect after surgery, and no recurrence tendency was found in the follow-up of 2years.Conclusions:For a large solitary mass with slow growth and no malignant clinical manifestations for a long time, clinicians can not rule out the hypothetical diagnosis of neurofibroma, even though its growth site is very rare, such as this case of a huge tumor located in the groin. For neurogenic tumors, early operation should be performed, and the prognosis of patients after tumor resection isexcellent.


2019 ◽  
Vol 2019 (9) ◽  
Author(s):  
Daiki Morita ◽  
Hitoshi Nemoto ◽  
Tomoichiro Togo ◽  
Naohiro Kimura ◽  
Yoshinori Ito

Abstract Resection of giant neurofibroma in neurofibromatosis type 1 has a high risk of perioperative bleeding because the tumors are enriched in blood vessels, which are weakened due to the loss and thinning of vascular smooth muscle. Therefore, we combined skin ligation around the tumor and use of an argon beam coagulator (ABC) for hemostasis during resecting the giant neurofibroma. The ABC is a non-contact-type hemostasis device employing argon gas as a medium. We examined the usefulness of our method by retrospectively comparing the outcomes of the ABC-use group with those of the non-use group (7 patients, 9 tumors). Although there was no difference in resected tumor weight between the two groups, the operation time was slightly shorter and the volume of blood loss was smaller in ABC-use group than in the non-use group. Our method for hemostasis is easy and safe and is considered to be a useful method.


2019 ◽  
pp. 75-78
Author(s):  
N.M. Fomenko ◽  
◽  
O.B. Synoverska ◽  
O.L. Tsymbalista ◽  
Z.V. Vovk ◽  
...  

2018 ◽  
Vol 9 (3) ◽  
pp. 329-330
Author(s):  
Ouiame El Jouari ◽  
Salim Gallouj ◽  
Safae Zinoune ◽  
Hanane Baybay ◽  
Fatima Zahra Mernissi
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