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1.
Pediatr Dermatol ; 32(4): e136-9, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25847574

RESUMEN

Idiopathic facial aseptic granuloma (IFAG), originally termed pyodermite froide du visage, describes a generally asymptomatic facial nodule presenting in childhood with clinical resemblance to pyoderma or cystic, granulomatous, or vascular lesions. Clinical understanding is constantly evolving, with recent observations indicating that IFAG may represent a subtype of childhood rosacea. We present a case of IFAG associated with eyelid chalazions in a 19-month-old boy. Although his clinical course paralleled previously reported IFAG cases, we observed a unique ultrasound variation during initial diagnostic examination. Further delineation of clinical, imaging, and histologic properties of IFAG may reveal insights into etiologic associations and ideal management.


Asunto(s)
Dermatosis Facial/diagnóstico por imagen , Granuloma/diagnóstico por imagen , Antiinfecciosos/uso terapéutico , Biopsia , Chalazión/diagnóstico , Diagnóstico Diferencial , Dermatosis Facial/tratamiento farmacológico , Dermatosis Facial/patología , Granuloma/tratamiento farmacológico , Granuloma/patología , Humanos , Lactante , Masculino , Metronidazol/uso terapéutico , Rosácea/diagnóstico , Piel/patología , Ultrasonografía
2.
Am J Forensic Med Pathol ; 28(2): 121-7, 2007 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-17525561

RESUMEN

The fetus is subjected to mechanical forces during labor and delivery, which may result in traumatic injuries. Such injuries include intracranial hemorrhage, spinal cord lesions, cephalhematoma, cranial or peripheral nerve palsies, intraabdominal organ rupture, or bony fractures. Risk for perinatal trauma and mortality is increased in primigravidas, multiple gestations, abnormal presentations, maternal-fetal disproportion, oligohydramnios, forceps or vacuum extractions, and internal version maneuvers. Very-low-birth-weight neonates (<1500 g) are at high risk due to ease of deformity of the cranium. Infants with certain congenital anomalies or pathologic processes that distort normal anatomy are also at increased risk, especially when a prenatal diagnosis is lacking. The authors present a case of a term gestation neonate who sustained a cervical spine dislocation fracture of C5-7, with subtotal transection of the spinal cord and resultant paralysis. The fetus was in vertex presentation, and a manual vaginal delivery was attempted. When the infant lodged in the birth canal following a difficult delivery of the head and arms, its enlarged abdomen was palpated, and the delivery was converted to an emergent cesarean section. The infant lived for 3 days and then expired due to neurologic complications of trauma sustained during the attempted vaginal delivery. Autopsy revealed a previously undiagnosed intraabdominal immature teratoma. The pathology of teratomas, the most common neonatal tumor and occasionally implicated in cases of birth trauma, will be addressed, followed by a review of the literature concerning birth trauma.


Asunto(s)
Neoplasias Abdominales/complicaciones , Traumatismos del Nacimiento/etiología , Teratoma/complicaciones , Adulto , Vértebras Cervicales/lesiones , Cesárea , Urgencias Médicas , Resultado Fatal , Femenino , Patologia Forense , Humanos , Recién Nacido , Complicaciones del Trabajo de Parto/etiología , Parálisis/etiología , Embarazo , Traumatismos de la Médula Espinal/etiología , Fracturas de la Columna Vertebral/etiología
3.
Am J Forensic Med Pathol ; 28(2): 116-20, 2007 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-17525560

RESUMEN

Neuroleptic malignant syndrome (NMS) is a diagnosis of exclusion difficult to make due to a lack of pathognomonic features. Diagnosing NMS by postmortem examination becomes increasingly challenging when possible underlying brain pathology is obscured. The diagnosis is based on clinical history and laboratory findings. Autopsy and histologic findings, if any, usually are reflective of hyperthermia or complications (eg, aspiration pneumonia) of NMS. The authors describe a case of a 36-year-old Hispanic woman with a presumptive diagnosis of pseudoseizures, treated with various combinations of neuroleptic medications over a 6-week period prior to her sudden, unexpected, in-hospital death. Neuroleptic malignant syndrome is likely to have contributed to this patient's death. Confounding factors and medicolegal issues of a postmortem diagnosis of NMS are discussed.


Asunto(s)
Síndrome Neuroléptico Maligno/diagnóstico , Lesión Renal Aguda/etiología , Adulto , Anticonvulsivantes/efectos adversos , Encéfalo/patología , Creatina Quinasa/sangre , Deshidratación/etiología , Femenino , Fiebre/etiología , Medicina Legal , Humanos , Hipovolemia/etiología , Fallo Hepático Agudo/etiología , Rigidez Muscular/etiología , Psicotrópicos/efectos adversos , Temblor/etiología
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