ABSTRACT
A 7-year-old boy suffered blunt multiple injuries to the head, face, chest, and abdomen in a motor vehicle accident. On admission he had impaired consciousness and dyspnea. Radiographic studies revealed facial fracture and pulmonary contusion. Shortly after admission, he fell into shock due to intraabdominal bleeding. Laparotomy revealed spleen rupture. His vital signs remained unstable and bloody drainage from the abdominal cavity continued after surgery. Computed tomography showed traumatic intracerebral hematoma in the right temporal lobe, enlarging and compressing the brainstem. Abdominal reoperation was performed first to control the bleeding and stabilize the hemodynamics, disclosing renal laceration. Then evacuation of the intracerebral hematoma and decompressive craniectomy was performed. Postoperatively, his hemodynamics were stabilized. Clinical course was uneventful and neurological deficits gradually improved. Three months after the trauma, the patient was discharged on foot. This case emphasizes the importance of hemodynamic stability in decisions of neurosurgical indication and timing in patients with multiple trauma including head injury.
Subject(s)
Brain Injuries/surgery , Cerebral Hemorrhage, Traumatic/etiology , Craniotomy , Decompression, Surgical , Multiple Trauma/surgery , Accidents, Traffic , Brain Injuries/diagnostic imaging , Brain Injuries/etiology , Brain Stem/physiopathology , Cerebral Hemorrhage, Traumatic/surgery , Child , Facial Bones/injuries , Hemodynamics , Hemoperitoneum/etiology , Humans , Laparotomy , Male , Reoperation , Skull Fractures/etiology , Splenic Rupture/etiology , Splenic Rupture/surgery , Temporal Lobe/injuries , Time Factors , Tomography, X-Ray Computed , Wounds, Nonpenetrating/surgeryABSTRACT
A 71-year-old woman who had undergone a total abdominal hysterectomy and pelvic irradiation for cervical cancer and fecal diversion for adhesive ileus was referred to us for a "left" ureteral stone and intermittent gross hematuria. Bilateral ureteral stents had been indwelled because of lower ureteral strictures for a long time. Hematuria continued after the removal of the ureteral stone, and she once went into hypovolemic shock at the time of exchange of the right ureteral catheter. Selective arteriography revealed a "right" ueteroarterial fistula. Endovascular management alone failed to resolve the fistula, but a subsequent transurethral metal coil embolization was effective, and the hematuria was relieved. She is still free from disease at 7-month followup. As far as we know, there has been no previous report of a transurethrally managed ureteroarterial fistula.
Subject(s)
Embolization, Therapeutic/methods , Fistula/therapy , Iliac Artery , Ureteral Diseases/therapy , Urinary Fistula/therapy , Aged , Female , Follow-Up Studies , Hematuria/etiology , Hematuria/therapy , Humans , Treatment Outcome , UrethraABSTRACT
A 44-year-old man presented with a rare case of idiopathic hypertrophic cranial pachymeningitis manifesting as generalized seizure. Neuroimaging and pathological examinations showed the typical features of hypertrophic cranial pachymeningitis. Tuberculosis was a possible cause based on the positive purified protein-derived skin test, but the origin of the disease was not confirmed by further examinations. Cerebral angiography showed total occlusion of the dural sinuses with development of the emissary veins. Histological examination of the dura showed thickening of the fibrous tissue with rare inflammatory cells, suggestive of the extremely long duration of the disease. The diagnosis was idiopathic hypertrophic cranial pachymeningitis, but was treated only with anticonvulsants. The disease did not progress during follow up of 3 years. Idiopathic hypertrophic cranial pachymeningitis may have various causes related to unusual forms of infectious or autoimmune disorders.
