Right lower quadrant pain in children caused by omental infarction.

BACKGROUND: Omental infarction is a rare cause of abdominal pain, with fewer than 300 cases reported in the literature. Only 15% of reported cases occur in the pediatric population. We present our experience with 18 children diagnosed with omental infarction admitted to Texas Children's Hospital over a 15-year period. STUDY DESIGN: A retrospective review of clinical records, diagnostic images, and pathologic findings was carried out for all children diagnosed with isolated omental infarction from 1986 to 2000 in order to analyze presenting signs and symptoms, preoperative imaging, surgical management, and postoperative outcomes. RESULTS: Eighteen children were treated for isolated omental infarction. There were 12 boys and 6 girls with an average age of 7.5 years (range 2 to 13). All patients presented with acute onset of right lower quadrant pain. Only 5 of 18 (24%) had associated gastrointestinal symptoms. The average temperature at presentation was 99.4 degrees F (+/- 0.78). The average white blood cell count was 11.4 (+/- 4.4). Fourteen patients had ultrasonographys performed preoperatively: 6 of 14 incorrectly diagnosed appendicitis, 4 of 14 were nondiagnostic and 4 of 14 correctly diagnosed omental infarction. Two of 18 patients underwent computed tomography scans, which were diagnostic for omental infarction. Resection of the infarcted omentum was performed in all patients and appendectomy in 16 of 18. Thirteen patients underwent an open procedure, 5 were performed laparoscopically. There were no postoperative complications. All patients had resolution of pain postoperatively and were discharged an average of 3.0 (+/- 0.9) days after admission. CONCLUSIONS: Omental infarction is an uncommon cause of right lower quadrant pain in children and is often diagnosed as appendicitis preoperatively. Ultrasonography and computed tomography can be diagnostic. Surgical resection of the infarcted omentum results in immediate resolution of pain with no morbidity.

Sonographic appearance of omental infarction in children.

BACKGROUND: Omental infarction has been previously reported in the adult surgical and imaging literature; however, the imaging features of this entity in children have received little attention. OBJECTIVE: The purpose of our study was to identify the sonographic features of omental infarction in nine children who had preoperative sonography and surgically proven omental infarction. MATERIALS AND METHODS: Sonographic images were reviewed and correlated with clinical information obtained from the patients' medical records, including clinical presentation, operative notes, and pathology reports. RESULTS: In seven of the children, sonography demonstrated a focal area of moderately increased echogenicity in the omental fat in the right abdomen (a previously described finding in omental infarction). This was an isolated finding in four of these cases. In the three cases where this was not an isolated finding, the more complex sonographic appearance led to incorrect preoperative imaging diagnoses. This finding of increased echogenicity in the omental fat was not present in the two remaining patients. CONCLUSION: Our study confirms that foci of moderately increased echogenicity in the omentum of the right abdomen, a sonographic finding described in omental infarction in a large series in adults (and in a single prior case report in children), can be seen in children as well. However, although this is a relatively unique finding, it may be absent in some cases or may be seen in conjunction with other sonographic findings which may preclude the correct preoperative sonographic diagnosis.

Renal venous thrombosis complicating acute myeloid leukemia with hyperleukocytosis.

PURPOSE: Leukemic hyperleukocytosis may cause organ- or life-threatening complications. Patients at highest risk appear to be those with acute myeloid leukemia (AML). Blast cell aggregation and thrombus formation in the microvasculature most commonly involves the central nervous system and the pulmonary circulation. We describe a child with AML and renal venous thrombosis (RVT), a previously unreported complication of hyperleukocytosis. PATIENTS AND METHODS: A 17-month-old boy had a white blood cell count of 103 X 10(9) cells/L and RVT (hematuria, arterial systolic hypertension, unilateral nephromegaly, poor renal venous blood flow) at diagnosis of acute myelomonocytic leukemia (AML, FAB M4). CONCLUSION: This case emphasizes the danger of hyperleukocytosis in AML and demonstrates that there may be other organ system dysfunction in addition to the well-described central nervous system and pulmonary complications. Renal venous thrombosis should be considered in the patient with leukemic hyperleukocytosis, hematuria, arterial hypertension, and appropriate radiographic findings. Aggressive cytoreductive measures should be pursued in such cases.

Epiglottitis following preparation for allogeneic bone marrow transplantation.

We describe a 7-year-old boy who developed acute, airway-threatening, non-infectious epiglottitis following high-dose cytosine arabinoside and total body irradiation preparative regimen for allogeneic BMT. Unlike gastrointestinal symptoms and oropharyngeal mucositis, acute epiglottitis is a previously unreported early complication following allogeneic BMT preparation. The pathogenesis of epiglottitis in our patient was presumably multifactorial, resulting from the combination of chemotherapy and irradiation. We recommend that this diagnosis be considered in the differential diagnosis of patients with significant upper airway symptoms following BMT preparation.