scholarly journals Malignant peripheral nerve sheath tumor of anterior abdominal wall- A rare presentation

2021 ◽  
Vol 3 (3) ◽  
pp. 81-83
Author(s):  
Benny P B ◽  
T A Vasu ◽  
Illakia Selvan ◽  
Anjali Rajan

Malignant peripheral nerve sheath tumor is highly malignant tumors that occur most commonly in head and neck as well as extremities. Very rarely it seen in the retroperitoneum. When associated with neurofibromatosis, they are having a poor outcome. We present a case malignant peripheral nerve sheath tumor of anterior abdominal wall. The location and rapid increase in size of the swelling permitted early diagnosis and treatment.

2001 ◽  
Vol 36 (12) ◽  
pp. 1866-1868 ◽  
Author(s):  
Pelin Oğuzkurt ◽  
Fazilet Kayaşelcuk ◽  
I.Serdar Arda ◽  
Özlem Barutçu ◽  
Ilhan Tuncer ◽  
...  

2013 ◽  
Vol 104 (5) ◽  
pp. 663-666
Author(s):  
Tomoyuki Tatenuma ◽  
Ryoko Sakata ◽  
Shinpei Sugiura ◽  
Takehiro Tajiri ◽  
Toshikazu Gondo ◽  
...  

2020 ◽  
pp. 014556131989764 ◽  
Author(s):  
Anju Chen ◽  
Tiantian Wang ◽  
Xianfa Xu

Malignant peripheral nerve sheath tumor (MPNST) is a malignant soft tissue sarcoma with high mortality, low morbidity, and poor prognosis. The MPNST occurs mostly in the limbs and torso, and rarely in the head and neck. However, MPNST is insensitive to radiotherapy and chemotherapy, and complete surgical resection with negative margin is the most important and effective strategy. We present a case of MPNST in the head and neck. The tumor invades the left temporal bone, petrous bone, and mastoid bone, and compression changes in the focal cerebellum and sigmoid sinus. The patient underwent the left temporal region tumor resection + surgical reconstruction with temporalis muscle flap and pectoralis major myocutaneous flap. Adjuvant radiotherapy (55 Gy) was given after surgery, and there were no local recurrence and distant metastasis after 31-month follow-up.


Rare Tumors ◽  
2014 ◽  
Vol 6 (4) ◽  
pp. 140-142 ◽  
Author(s):  
Babusha Kalra ◽  
Pamela Alice Kingsley ◽  
Harinder Singh Bedi ◽  
Kanwardeep Singh Kwatra ◽  
Preeti Negi

2017 ◽  
Vol 2017 ◽  
pp. 1-4
Author(s):  
Marija Milković Periša ◽  
Tihana Džombeta ◽  
Jasminka Stepan Giljević ◽  
Božo Krušlin

Benign and malignant tumors are common in the setting of neurofibromatosis type 1 (NF1). Malignant peripheral nerve sheath tumor (MPNST) and angiosarcoma are rare tumors in children and adolescents and mostly occur in young patients in relation to NF1. Both histological types can be present in the same tumor mass in patients with NF1. We present a case of 12.5-year-old girl with NF1 who first presented with MPNST of the right inguinal region and 1.5 years later with unrelated angiosarcoma of the scalp.


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