UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 熱傷再建の原則：手術の概要 principles of burn reconstruction overview of surgical procedures

English Journal

Erythroderma desquamativa of Leiner (clinical case).

Tsiskarishvili N1, Tsiskarishvili Ts.Author information 1Tbilisi State Medical University, Department of Dermatology and Venereology, Georgia.AbstractNewborn at the age of 1 month and 10 days was examined in our Department in accordance with the request of Children's Hospital pediatrician for a diagnosis and prescription of adequate treatment. Anamnesis revealed that the child was born from parents (the second child) who are close relatives to each other (cousins, the Muslims - inbreeding). According to parents, the first child was born healthy, grow and develop without pathological abnormalities. At the birth of their second child, the changes in baby's skin appeared a month after birth. According to the father, during pregnancy, the baby's mother was injured (falling) followed by removal of hemorrhagic fluid from the pelvic cavity. On admission to our Department, the whole skin of newborn was brightly hyperemic, infiltrated and heavily shelled. On the scalp there were concentrations of yellow-gray color "fat" scales, resembling the bark or shell, going down on the forehead and brow. A child's face had masklike appearance. In some locations, in the parietal and frontal regions, after the removal of flakes the baldness was observed. The folds of the lower body (perineum, buttocks) were swollen, brightly hyperemic, macerated and soaked. In the middle of the folds were deep, difficult to heal fractures.
Georgian medical news.Georgian Med News.2011 Jun;(195):51-4.
Newborn at the age of 1 month and 10 days was examined in our Department in accordance with the request of Children's Hospital pediatrician for a diagnosis and prescription of adequate treatment. Anamnesis revealed that the child was born from parents (the second child) who are close relatives to ea
PMID 21778541

Bilateral mandibular condylysis from systemic sclerosis: case report of surgical correction with bilateral total temporomandibular joint replacement.

Doucet JC1, Morrison AD.Author information 1Oral and Maxillofacial Surgery, Dalhousie University, Halifax, Nova Scotia, Canada.AbstractSystemic sclerosis (SSc) is a multisystem connective tissue disease of unknown etiology. The hallmark of SSc is scleroderma, referring to the presence of thickened, hardened skin. Oral and maxillofacial manifestations of the disease are numerous including masklike appearance, trismus, muscular atrophy, thin atrophied lips, secondary microstomia, xerostomia, rigidity of tongue and lips, widening of the periodontal ligament space, trigeminal neuralgia, and resorption of the mandible. A 35-year-old woman with limited cutaneous SSc presented with bilateral mandibular condylysis, severe class II mandibular deficiency, and large anterior open bite and limited range of mandibular opening at 27 mm. Surgical correction consisted of bilateral total temporomandibular joint reconstruction with stock prostheses combined with Le Fort I maxillary impaction and functional advancement genioplasty. This resulted in a functional occlusion with elimination of her open bite and a more esthetic profile. Her occlusion has remained stable at 7 months. The incidence of mandibular resorption in SSc has been found to be 20% to 33%. The mandibular angles are most commonly involved (37.6%), followed by the condyle (20.8%), coronoid process (20.0%), and the posterior border of the ascending ramus (14.4%). Bilateral condylysis is present in 13.7% of the cases. Very few cases of surgical correction of malocclusion induced by SSc-related condylysis have been reported in the literature. To the best of our knowledge, this is the first case report of bilateral condylysis from SSc where surgical replacement of the resorbed condyles was attempted. Bilateral total temporomandibular joint replacement can give these patients a functional occlusion, improved facial balance, and improved quality of life.
Craniomaxillofacial trauma & reconstruction.Craniomaxillofac Trauma Reconstr.2011 Mar;4(1):11-8. doi: 10.1055/s-0031-1272904.
Systemic sclerosis (SSc) is a multisystem connective tissue disease of unknown etiology. The hallmark of SSc is scleroderma, referring to the presence of thickened, hardened skin. Oral and maxillofacial manifestations of the disease are numerous including masklike appearance, trismus, muscular atrop
PMID 22379502

Parkinsonism due to predominant involvement of substantia nigra in Japanese encephalitis.

Pradhan S1, Pandey N, Shashank S, Gupta RK, Mathur A.Author information 1Department of Neurology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.AbstractOBJECTIVE: To study the clinical correlates of lesions seen predominantly in the substantia nigra in some patients with Japanese encephalitis (JE).
Neurology.Neurology.1999 Nov 10;53(8):1781-6.
OBJECTIVE: To study the clinical correlates of lesions seen predominantly in the substantia nigra in some patients with Japanese encephalitis (JE).BACKGROUND: JE typically involves thalamus, brainstem, spinal cord, and cerebral cortex. Rarely, basal ganglia and cerebellum may be affected. Lesions ar
PMID 10563628