scholarly journals Paraneoplastic opsoclonus myoclonus syndrome associated with inflammatory myofibroblastic tumor in a pediatric patient

2020 ◽  
Vol 67 (8) ◽  
Author(s):  
Karyn Gerstle ◽  
Amir Siddiqui ◽  
Jefree J. Schulte ◽  
Susan L. Cohn
Keyword(s):  
Pediatric Patient ◽  
Inflammatory Myofibroblastic Tumor ◽  
Opsoclonus Myoclonus Syndrome

scholarly journals Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Miriam Harel ◽  
John H. Makari
Keyword(s):  
Pediatric Patient ◽  
Inflammatory Myofibroblastic Tumor ◽  
Wide Excision ◽  
Adenomatoid Tumor ◽  
Complete Excision ◽  
Paratesticular Mass

Although rare, paratesticular inflammatory myofibroblastic tumor (IMT) represents the second most common paratesticular mass after adenomatoid tumor and comprises roughly 6% of such lesions. Only approximately four cases have been reported in patients younger than 18 years of age. We report an incidentally discovered paratesticular IMT in a 17-year-old male successfully treated with wide excision and testis sparing. To our knowledge, no recurrence has been reported after complete excision of paratesticular IMT; however, continued follow-up is recommended.

scholarly journals Inflammatory Myofibroblastic Bladder Tumor in a Patient with Wolf-Hirschhorn Syndrome

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Antonio Marte ◽  
Paolo Indolfi ◽  
Carmine Ficociello ◽  
Daniela Russo ◽  
Matilde Oreste ◽  
...  
Keyword(s):  
Urinary Bladder ◽  
Head And Neck ◽  
Pediatric Patient ◽  
Inflammatory Myofibroblastic Tumor ◽  
Bladder Tumor ◽  
Genitourinary System ◽  
Rare Neoplasm ◽  
True Neoplasm

Inflammatory myofibroblastic tumor (IMT) is a rare neoplasm described in several tissues and organs including genitourinary system, lung, head, and neck. The etiology of IMT is contentious, and whether it is a postinflammatory process or a true neoplasm remains controversial. To our knowledge, we report the first reported case of IMT of urinary bladder in a pediatric patient with Wolf-Hirschhorn (WHS). We also review the literature about patients with associated neoplasia.

Steroid treatment for pancreatic inflammatory myofibroblastic tumor in a pediatric patient: Case report

Pancreatology ◽  
2017 ◽  
Vol 17 (4) ◽  
pp. S46-S47
Author(s):  
Carlos Mac ◽  
Lelio Ciciliani ◽  
Alejandrina Cripovich ◽  
Mariana Bernaus
Keyword(s):  
Case Report ◽  
Pediatric Patient ◽  
Inflammatory Myofibroblastic Tumor ◽  
Steroid Treatment ◽  
Patient Case

Rare Endobronchial Inflammatory Myofibroblastic Tumor in Pediatric Patient Detected on PET/CT Imaging

2017 ◽  
Vol 42 (9) ◽  
pp. e407-e408
Author(s):  
Pelin Ozcan Kara ◽  
Zehra Pinar Koc ◽  
Elvan Caglar Citak ◽  
Ali Nayci ◽  
Gokhan Berktug Bahadir ◽  
...  
Keyword(s):  
Pediatric Patient ◽  
Inflammatory Myofibroblastic Tumor ◽  
Ct Imaging ◽  
Pet Ct

Foreign bodies in the pediatric patient

1998 ◽  
Vol 35 (4) ◽  
pp. 271-378 ◽  
Author(s):  
D JOHNSON ◽  
V CONDON
Keyword(s):  
Pediatric Patient ◽  
Foreign Bodies
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