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J J Chiaro

Publications and source records attributed to J J Chiaro.

3 recordsLinked to original sources

Chylothorax as a manifestation of child abuse.

OBJECTIVE: Chylothorax presenting in a child without a well defined etiology may be a manifestation of child abuse. We recently observed a child with bilateral chylothoraces who demonstrated coexisting nonaccidental injuries. It is our intention to alert physicians to the association of chylothorax with nonaccidental trauma and review the prior medical literature. DESIGN: Case report. SETTING: Pediatric emergency department and intensive care unit. PATIENT: An 18-month-old female child who presented with respiratory distress and failure to thrive. INTERVENTIONS: Diagnostic and therapeutic thoracentesis. Skeletal survey and radionuclide bone scan. Nutritional support. OUTCOME MEASURES: Pleural fluid is characterized as chylous if it contains significant numbers of lymphocytes and lipid. Unexplained fractures of the ribs and long bones in varying stages of healing are considered nonaccidental. Failure to thrive may be considered nonorganic when nutritional support alone results in significant weight gain. RESULTS: Our patient presented with respiratory distress of one-week duration and failure to gain weight during the prior five months. The chest radiograph demonstrated bilateral pleural effusions, which were aspirated. The aspirate contained 1733 cells/mm3 (98% lymphocytes), which were lipid laden. The triglyceride concentration was 806 mg/dl. A skeletal survey demonstrated bilateral first rib, clavicle, and ulnar fractures. A radionuclide bone scan additionally revealed multiple vertebral body fractures. Nutritional support alone resulted in significant weight gain. The patient was reported to local authorities as having been abused. CONCLUSION: Child abuse should be considered as an etiology for cryptogenic chylothorax. Further studies should be undertaken in this circumstance to search for coexisting injuries, which may indicate nonaccidental trauma.

Child Abuse↗

Autosomal dominant hypoparathyroidism with variable, age-dependent severity.

Hypoparathyroidism (hypocalcemia, hyperphosphatemia, mild hypomagnesemia, and inappropriately low serum C-terminal parathyroid hormone concentration) was found in six members of a family representing three successive generations. No patient had aortic arch or conotruncal malformations, lymphopenia, or features of type I or type II autoimmune polyglandular syndromes. Two individuals had transient neonatal seizures without further difficulties despite persistent hypocalcemia. None of the four affected adults has had major complications of hypoparathyroidism (mental retardation, cataracts, or seizures). We believe that persistence of hypoparathyroidism after resolution of neonatal hypocalcemic seizures should prompt a survey of the family for hypoparathyroidism.

Adult↗