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| Journal:
INTERNATIONAL JOURNAL OF PEDIATRICS
MAY 2018
, Volume 6
, Number 5 (53); Page(s)
7639
To
7640. |
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| Paper:
Management Of Perinatal Testicular Torsion: A Single Centre Experience
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| Author(s):
Zouari Mohamed, Louati Hamdi*, Dhaou Mahdi Ben, Abid Imen, Mhiri Riadh
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| * DEPARTMENT OF PEDIATRIC SURGERY, HEDI CHAKER HOSPITAL, 30219 SFAX, TUNISIA |
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| Abstract:
Dear Editor-in-Chief, Perinatal testicular torsion (PTT) is a rare entity, occurring in 1: 7500 newborns (1). It accounts for about 12% of all cases of torsion throughout childhood and is considered almost always extravaginal in origin (2). Although PTT is widely accepted to be an antenatal event, the exact timing and duration of torsion are not known (3). Perinatal testicular torsion usually presents as a bluish-black discolouration of the scrotum associated with a scrotal swelling, which is non-transilluminable. However, due to an important variation in clinical presentation, this condition remains unrecognized in many patients and may be missed or confused with other conditions (4). The management of PTT is controversial, due to the low viability of the testis and the possibility of bilateral torsion (5-7). This is a review of our experience with six cases of PTT, highlighting diagnostic and therapeutic difficulties of this condition. From January 2010 to June 2017, we treated five newborns with PTT (right side [n=2], left side [n=2], bilateral [n=1]). Their mean birth weight was 3.2 kg (range, 2.8-3.8 kg). Their age at presentation ranged from 2 hours to 6 days (mean, 38 hours). Doppler ultrasonography was performed in four patients, and was inconclusive in all cases. All patients underwent emergency exploration and found to have extravaginal torsion of testes. The patient with bilateral PTT had black, hemorrhagic and necrotic testes (Figure.1).Bilateral orchiopexy was performed after detorsion. At 3-month-old, both testes were viable and were in the normal position in the scrotum. In one patient with unilateral PTT, the torsed testis was ischemic but not frankly necrotic, so it was preserved, but on follow-up, it was found atrophic. In the remaining three patients, the testes were frankly necrotic; they were treated with orchiectomy and contralateral orchiopexy. On histology, the removed testes were totally necrotic without any viable testicular tissue. Perinatal testicular torsion is often difficult to diagnose mostly due to an important variation in clinical presentation. A high degree of suspicion is required for early diagnosis and management of this condition. Immediate emergency surgery is increasingly advocated for PTT in the hope of saving the testis (1, 7). Therefore, it is a reasonable option to leave in place even necrotic testis, whenever possible, as some testicular function may still be possible (4).
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| Keyword(s): NEONATE, PERINATAL, TESTICULAR TORSION, TUNISIA |
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+ Click to Cite.
APA: CopyZOUARI, M., & LOUATI, H., & DHAOU, M., & ABID, I., & MHIRI, R. (2018). MANAGEMENT OF PERINATAL TESTICULAR TORSION: A SINGLE CENTRE EXPERIENCE. INTERNATIONAL JOURNAL OF PEDIATRICS, 6(5 (53)), 7639-7640. https://www.sid.ir/en/journal/ViewPaper.aspx?id=572936 Vancouver: CopyZOUARI MOHAMED, LOUATI HAMDI, DHAOU MAHDI BEN, ABID IMEN, MHIRI RIADH. MANAGEMENT OF PERINATAL TESTICULAR TORSION: A SINGLE CENTRE EXPERIENCE. INTERNATIONAL JOURNAL OF PEDIATRICS. 2018 [cited 2022May21];6(5 (53)):7639-7640. Available from: https://www.sid.ir/en/journal/ViewPaper.aspx?id=572936 IEEE: CopyZOUARI, M., LOUATI, H., DHAOU, M., ABID, I., MHIRI, R., 2018. MANAGEMENT OF PERINATAL TESTICULAR TORSION: A SINGLE CENTRE EXPERIENCE. INTERNATIONAL JOURNAL OF PEDIATRICS, [online] 6(5 (53)), pp.7639-7640. Available: https://www.sid.ir/en/journal/ViewPaper.aspx?id=572936.
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Yearly Visit 42
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