x
Filter:
Filters applied
- Online Exclusives
- Biondini, DiegoRemove Biondini, Diego filter
- Journal of Pediatric SurgeryRemove Journal of Pediatric Surgery filter
Online Exclusives
4 Results
- Rapid Communication
A case of frozen pelvis: Primary actinomycosis of urinary bladder in a young boy
Journal of Pediatric SurgeryVol. 47Issue 12e9–e11Published in issue: December, 2012- Maria Anastasia Bianchini
- Eleonora Bigi
- Paolo Repetto
- Pierluca Ceccarelli
- Viviana Durante
- Diego Biondini
- and others
Cited in Scopus: 2We report a case of urinary bladder actinomycosis in childhood. In children abdominal actinomycosis is rare and unlikely involves the urinary tract, so it is often misdiagnosed. An 7-year-old boy was referred to a secondary level hospital because of abdominal pain and dysuria. Physical examination revealed a left hypochondrial mass. Hypothesizing a pelvic rhabdomyosarcoma, a biopsy with mini-laparotomy access was performed. The first histopathological analysis did not show any malignant cells, and a 14-day antibiotic course was ineffective. - Research Article
Bilateral xanthogranulomatous funiculitis and orchiepididymitis in a 13-year-old adolescent boy
Journal of Pediatric SurgeryVol. 47Issue 10e33–e35Published in issue: October, 2012- Paolo Repetto
- Maria Anastasia Bianchini
- Pier Luca Ceccarelli
- Luca Roncati
- Viviana Durante
- Diego Biondini
- and others
Cited in Scopus: 6Xanthogranulomatous orchitis is an extremely rare inflammatory nonneoplastic lesion of the testis. We report a case of a 13-year-old adolescent boy who presented a painless left hemiscrotal swelling. The subsequent ultrasonography and magnetic resonance imaging revealed the presence of abnormal expanding tissue located in both testes and spermatic cord, reaching the internal inguinal ring. Testicular tumor markers were normal. The frozen section examination of the surgical specimen showed only inflammatory tissue and not neoplastic tissue. - Rapid Communication
Jejunal obstruction as initial presentation of polyarteritis nodosa in a 13-month-old boy
Journal of Pediatric SurgeryVol. 46Issue 7e27–e29Published in issue: July, 2011- Andrea Venuta
- Pier Luca Ceccarelli
- Diego Biondini
- Federica Montanari
Cited in Scopus: 11Systemic polyarteritis nodosa (PAN) is a rare disease in childhood affecting small and midsized arteries. The typical presentation in children is of isolated 1- or 2-organ involvement, and the diagnosis is often based on the histopathology. We report a case of pediatric PAN whose presenting symptom was jejunal obstruction owing to ischemic necrosis of the small bowel. The postoperative recovery was uneventful, and the patient responded well to steroid therapy. There are only a few cases of PAN with intestinal involvement described in the literature, some of them fatal. - Rapid Communication
Three small testes in left hemiscrotum: a rarer caseof polyorchidism
Journal of Pediatric SurgeryVol. 45Issue 2e21–e23Published in issue: February, 2010- Paolo Repetto
- Pierluca Ceccarelli
- Anastasia Bianchini
- Viviana Durante
- Diego Biondini
- Alfredo Cacciari
Cited in Scopus: 11Polyorchidism is a rare congenital anomaly. A review of literature has yielded about 100 cases. We describe a rarer case of polyorchidism consisting of 3 testes on left hemiscrotum and one normal testis in right hemiscrotum. Diagnosis and management are discussed.