Torsion of an intrahydrocelic sac in a child: A case report
© Christianakis et al; licensee BioMed Central Ltd. 2008
Received: 19 May 2008
Accepted: 16 June 2008
Published: 16 June 2008
We report the case of a 3-yr-old boy who presented an acute right hydrocele. A rapid scrotal swelling under tension developed the first hours and the child complained for discomfort especially during palpation of the scrotum. Three days later, surgical exploration revealed an incomplete torsion of a communicated and pedunculated peritoneal sac arising from the tunica vaginalis testis.
The present case report represents the eleventh report of torsion of processus vaginalis saccular protrusion in the literature, being unique due to painless hematocele.
In the patent processus vaginalis the containing fluid or any of the intraabdominal organs is characterized as hydrocele or hernia respectively. Hernia or hydroceles sacs as well as the rare saccular protrusion of processus vaginalis (SPPV) are peritoneal protrusions. Histologically a single layer of mesothelial origin cells, lining the inner cyst surface and loose connective tissue in the parietals may be present. In several cases the parietals of a congenital hernia sac may contain some muscle fibers. In the literature only fourteen similar complicated SPPV cases in children [1–10] and one more in an adult woman have been presented furthermore .
Our case refers to a 3-year-old boy who presented to the emergency department, because of an acute sudden swelling of the right scrotum. Because of the swelling the child felt uncomfortable in palpation. The clinical examination revealed a trans-illuminated poorly encysted big hydrocele like a common cyst of spermatic cord in tension. The cyst was afebrile having bilateral cremasteric reflexes. As an infant, he had a big scrotal hydrocele on the right side, which gradually disappeared until the 15th month of his life. Blood and urine laboratory tests, in exception of elevated white blood cells (WBC: 15,000/μl) were normal.
The SPPVs, which are usually referred as intrahernial hydroceles or intrahydrocelic hernias, are fluid-filled sacs lying entirely within the hernias. Intrahernial or intrahydrocelic sacs are a more accurate term, because these entities containing fluid contents and are free hanging. They seem like simple serous cysts, with a short or long pedunculated stalk, communicating through a small hole, as in our case in the hanging part with the intrahydrocelic space.
The first who described a pedunculated cyst within the hernia sac, as a partial distal intussusception of a patent processus vaginalis, in a child, was Dr. Lockwood in 1896 . Lockwood had initially the same wrong impression to the authors of the present case report. Bloom DA et al and Perez LM et al on 1993 and 1999 respectively described three cases of intussuscepted patent processus vaginalis which was twisted [1, 2].
In the literature only eight cases referring to "torsion of an inguinal hernia" [2–7] and three more ''to torsion of a communicated hydrocele or benign cyst'' have been presented [8–10]. The vast majority of the presented cases refer to children except a unique report from Russia which describes torsion of an intrahernial cyst in an adult female patient . The containing fluid in all these congenital origin sacs was serous or bloody.
The SPPV most frequently lie just proximal to the scrotal inlet or close to the testis and it can produce discomfort or acute scrotum in cases that is tearing. For this reason they must be included in the differential diagnosis of suddenly appearing persistent hydroceles or acute scrotum in children. The severity of symptoms depends on the cyst's size and the existence and the pattern of the concomitant torsion. Long pedunculated small cysts are more predisposing in complete torsion. This fact is facilitating from the gravity, since the cyst is hanging from a firm point towards the bottom of the hydrocele sac, exactly as the clapper bell. Eleven out of the thirteen reported cases were presented with painful scrotal swellings, but two were painless enlargements, as in our case [7–9]. This is may be a possible explanation for the great number of undiagnosed transiently twisted SPPVs. In addition, these must be differentiated from the inguinal cystic lymphangiomas.
The preoperative clinical and ultrasound diagnosis in our case was difficult. The cyst was occupying almost the entire anatomical space of the tunica vaginalis without acute scrotum, because of partially twisting. In such cases bleeding may occur mainly from the external parietal vessels lying next to the cyst, although it is difficult to cause necrosis of the cyst. In all of the reported cases the patients did not present nausea, vomiting or abdominal pain, symptoms that are very common in children with testicular torsion.
In conclusion, the SPPVs are rare inguinal-scrotal pedunculated sacs which containing serous fluid. These are rather types of communicated, coexisting and non-classified hydroceles instead of hernias that lie in a hydrocelic or hernia sac. In very rare cases SPPVs can twist producing either uncomforting like hydroceles in tension or symptoms of acute scrotum.
Written consent was obtained from the patient, a copy is available from the editor in chief.
We thank the patient's relatives for permitting us to present the case as well as the photo material.
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