Cardiac tamponade caused by broken sternal wire after pectus excavatum repair: a case report.

Complications of pectus excavatum surgery include pneumothorax, pleuritis, hemothorax, pericardial effusion, displacement of bar, pericarditis and cardiac injury, etc. This is the case of a 15-year-old boy with cardiac tamponade caused by pericarditis who had taken the operation for a pectus excavatum repair one year previously. The cause was a sternal wire which was used for attachment of the bar to sternum that had fractured and migrated through the pericardium causing a pericardial injury and a pericarditis.

Unilateral hydronephrosis and hydroureter by foreign body in urinary bladder: a case report.

Foreign bodies inserted through the urethra are often found in the urinary bladder. We presently report the first case of hydronephrosis and hydroureter due to direct compression in the urinary bladder by silicon, which had been introduced by the patient himself 2 yr prior to presentation with severe right flank pain. Computed tomography indicated a convoluted, high-attenuation mass in the urinary bladder; unilateral hydronephrosis and hydroureter were also present due to direct compression by the mass. The foreign body was removed using a cystoscope. This foreign body was proven to be silicon.

Narrow duplicated or triplicated internal auditory canal (3 cases and review of literature): can we regard the separated narrow internal auditory canal as the presence of vestibulocochlear nerve fibers?

The narrow duplicated internal auditory canal (IAC) is a very rare malformation, and there is no report about the narrow triplicated IAC in the literature. It has been believed to be associated with congenital sensorineural hearing loss and to be a result of aplasia or hypoplasia of the vestibulocochlear nerve or the cochlear branch. We present 2 cases of unilateral narrow duplicated IAC and 1 case of unilateral narrow triplicated IAC with ipsilateral sensorineural hearing loss. The separated, accessory bony canals delineated on high-resolution computed tomography do not mean the presence of nerve fibers. In previously presented cases and in our case, the separated small canals were vacant and without a cochlear nerve fiber. We present new common radiological findings as follows: the bony canal to the cochlea is very thin and the connection with the modiolus of the cochlea is interrupted in narrow separated IAC.

Myeloid sarcoma of both kidneys, the brain, and multiple bones in a nonleukemic child.

A myeloid sarcoma (MS) is an extramedullary tumor consisting of primitive granulocytic precursor cells. Although most such tumors have been reported in patients with acute myelogenous leukemia, MS is rarely recognized as an isolated tumor without any evidence of leukemia. However, in such cases, the initial diagnosis of MS can be difficult, so initial misdiagnosis rates of up to 75% have been reported. This report describes an unusual case of MS in a 3-year 5-month-old girl presenting as bilateral renal enlargements, and brain masses, with multiple bone involvements, but no hematological abnormalities.