Attention deficit hyperactivity disorder in children with congenital heart diseases / 国际儿科学杂志

Congenital heart disease is the most common congenital defect.With the advancement of surgical techniques, the survival rate of children with congenital heart disease is gradually increasing.However, the neurodevelopmental defects in children with congenital heart disease have gradually increased, which elicits increasing scholars′ attention.Attention deficit hyperactivity disorder(ADHD)is one of the most prominent neurodevelopmental behavior disorders in children.In previous studies, the prevelance of ADHD in cyanotic congenital heart disease was obviously higher than that of the general population, and however, research of congenital heart disease was in its infancy.This paper intends to review the incidence, etiology, pathogenesis, treatment and prognosis of ADHD in congenital heart disease in order to provide references for clinical work.

Electrophysiologic Findings of Ulnar Neuropathy at the Elbow According to the Level of the Lesion

OBJECTIVE: To determine whether electrophysiologic findings of ulnar neuropathy at the elbow (UNE) are associated with anatomic location or a pathophysiologic mechanism, electrophysiologic findings of ulnar neuropathy above the elbow (UNAE) and below the elbow (UNBE) were compared. METHOD: Electrophysiologic findings of 56 patients with UNE were analyzed: segmental ulnar motor conduction study with abductor digiti quinti (ADQ) and first dorsal interosseous (FDI) recordings, ulnar and dorsal ulnar cutaneous nerve (DUCN) sensory action potentials, and needle electromyographic findings. Based on anatomic location, lesions were divided into UNAE and UNBE. Based on pathophysiologic findings, they were classified into three groups (focal demyelination, axonal degeneration, and mixed lesion). RESULTS: Twenty-eight patients were diagnosed with UNAE, and 28 with UNBE. Of the patients with UNAE, 4 had focal demyelination, 2 showed axonal degeneration, and 22 were of mixed lesions. Of patients with UNBE, 5 had focal demyelination, 6 showed axonal degeneration, and 17 were of mixed lesions. No significant differences in pathophysiologic mechanisms, or in electrophysiologic findings, were observed between UNAE and UNBE. The proportion of positive findings of focal demyelination was higher in FDI recording than in ADQ recording; however, this finding was not statistically significant (p>0.05). Thirty of 31 patients with abnormal DUCN had axonal degeneration with or without focal demyelination, whereas 9 of 25 patients with normal DUCN had focal demyelination only (p<0.05). CONCLUSION: Electrophysiologic findings did not relate to the anatomic location of UNE, but could relate to the pathophysiologic severity or fascicular involvement of the lesion.

Depression and Coronary Artery Disease(I): Pathophysiologic Mechanisms

Depression and coronary artery disease are both highly prevalent diseases. Many previous studies suggest that depression is a common comorbid condition in patients with coronary artery disease and has a significant negative impact on the onset, course, and prognosis of coronary artery disease. However, the exact mechanisms that underlie the association between these two diseases remain unclear. Pathophysiologic mechanisms that may explain the effect of depression on coronary artery disease include hypercoagulability, hypothalamus-pituitary-adrenal axis and autonomic nervous system dysregulation, altered inflammatory response. On the contrary, pathophysiologic mechanisms in coronary artery disease that affect depression are less well known. It is also suggested that both diseases may share a common genetic vulnerability. The authors reviewed the literature on the pathophysiologic relationships of depression and coronary heart disease.

Two Cases of Invasive Aspergillosis of Sino-nasal Origin

Cerebral aspergillosis is a rare condition that affects primarily the immunocompromised host. Most of cerebral aspergillosis is developed by hematogenous dissemination from extracranial foci, but aspergillosis of sino-nasal origin rarely affects the CNS. In case 1, wel symptom of tumor recurrence was unilateral numbness of the chin. A 65-year-old male was admitted because of paresthesia around the left chin and left lower lip. Neurologic examination revealed hypesthesia on the left side of chin, lower lip and buccal mucous mem-brane. Bone scan (Tc-99m MDP) showed focal hot uptakes on the left mandible and left first rib. Brain CT with bone window setting showed a focal osteolytic lesion in the bone marrow of the left mandibular canal without destruction of bone cortex. Both coronal T1 weighted image and axial T2 weighted image showed focal low signal intensities on the left ramus. The pathophysiologic mechanism could be understood by identification of the pathologic focus.

A Case of Numb-Chin Syndrome Assoicated with Hodgkin's Disease

The numb chin syndrome (NCS) is characterized by chin or lower lip numbness restricted to the distribution of the mental nerve (the distal trigeminal nerve). The authors report a patient whose initial symptom of tumor recurrence was unilateral numbness of the chin. A 65-year-old male was admitted because of paresthesia around the left chin and left lower lip. Neurologic examination revealed hypesthesia on the left side of chin, lower lip and buccal mucous mem-brane. Bone scan (Tc-99m MDP) showed focal hot uptakes on the left mandible and left first rib. Brain CT with bone window setting showed a focal osteolytic lesion in the bone marrow of the left mandibular canal without destruction of bone cortex. Both coronal T1 weighted image and axial T2 weighted image showed focal low signal intensities on the left ramus. The pathophysiologic mechanism could be understood by identification of the pathologic focus.