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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Der Pathologe 20 (1999), S. 365-370 
    ISSN: 1432-1963
    Keywords: Schlüsselwörter Restriktive Dermopathie ; Autosomal rezessive Genodermatose ; Fetale Akinesie/Hypokinesie-Deformationssequenz ; Arthrogryposis ; Polyhydramnion ; Key words Restrictive dermopathy ; Autosomal recessive genodermatosis ; Fetal akinesia/hypokinesia deformation sequence ; Arthrogryposis ; Polyhydramnios
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Restrictive dermopathy is a rare, fatal, autosomal recessive, congenital skin disease. Rigidity of translucent thin skin, which is thus highly vulnerable and tears, spontaneously causes intra-uterine fetal akinesia or hypokinesia deformation sequence (FADS), characteristic dysmorphic facies with fixed open mouth in O position, and generalized joint contractures (arthrogryposis). Polyhydramnios and pulmonary hypoplasia are distinctive manifestations, leading to respiratory insufficiency and premature delivery at about 31 weeks of gestation. We report on a case of a prematurely born infant who presented with the typical morphological features and describe the light- and electronmicroscopical findings as described in the literature.
    Notes: Zusammenfassung Die restriktive Dermopathie ist eine seltene autosomal rezessive letal verlaufende Genodermatose. Die Straffheit der dünnen, durchscheinenden, leicht einreißenden Haut bewirkt intrauterin Die „Fetale Akinesie bzw. Hypokinesie Deformation Sequenz” (FADS), eine charakteristische Fazies mit fixierter Gesichtsmorphe und O-förmig offenem Mund sowie Gelenkkontrakturen (Arthrogryposis). Dem Polyhydramnion folgt die stets vorzeitige Geburt etwa in der 31. SSW sowie pulmonale Hypoplasie und respiratorische Insuffizienz. Wir berichten über einen weiteren Fall eines Frühgeborenen mit den typischen klinisch-morphologischen Stigmata, beschreiben die licht- und elektronenmikroskopischen Befunde und diskutieren das Leiden vor dem Hintergrund der vorliegenden Literatur.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Langenbeck's archives of surgery 384 (1999), S. 44-49 
    ISSN: 1435-2451
    Keywords: Key words Cystic pancreatic tumors ; Cystadenoma ; Cystadenocarcinoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Introduction: Among the rare cystic pancreatic tumors, serous and mucinous cystadenoma and mucinous cystadenocarcinoma are most often diagnosed. Case: We report on a total of 21 patients with cystic neoplasms who underwent surgery, 11 of whom had mucinous cystadenocarcinoma. Of the 10 remaining patients, serous and mucinous cystadenoma were diagnosed in two groups of five. A common feature of all cystic neoplasms is slow growth, leading to clinical symptoms at an advanced stage, with tumors frequently becoming enormous. Results: In approximately half of the cases, diagnosis was possible by means of ultrasound, computed tomography and, in three instances, by preoperative percutaneous aspiration. Differential diagnosis of pseudocysts proved to be most difficult. Conclusion: Given the low operative risk, resection should always be performed in instances where findings cannot be clearly identified. Moreover, compared with ductal pancreatic carcinomas, the prognosis of a cystadenocarcinoma after early resection is extremely favorable, so that postponing resection might reduce the patient's prospects of being cured.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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