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Verfasst von:Krzossok, Stefan [VerfasserIn]   i
 Benck, Urs Tobias [VerfasserIn]   i
 Woude, Fokko J. van der [VerfasserIn]   i
 Braun, Claude [VerfasserIn]   i
Titel:Disseminierte intravasale Gerinnung, Perimyokarditis und bilaterales Pleuraempyem bei adultem Still-Syndrom
Paralleltitel:Disseminated intravascular coagulation, perimyocarditis and bilateral pleural empyema in adult Still's disease
Verf.angabe:S. Krzossok, U. Benck, F. J. van der Woude, C. Braun
Jahr:2004
Umfang:3 S.
Fussnoten:Gesehen am 31.05.2022
Titel Quelle:Enthalten in: Deutsche medizinische Wochenschrift
Ort Quelle:Stuttgart : Thieme, 1875
Jahr Quelle:2004
Band/Heft Quelle:129(2004), 47, Seite 2535-2537
ISSN Quelle:1439-4413
Abstract:HISTORY: A 21-year-old man was admitted to the hospital because of high fever, arthralgias and myalgias. One week before he was treated with penicillin G orally because of cough and sore throat. PHYSICAL EXAMINATION: The critically ill patient presented with a red throat and cervical lymphadenopathy. Lung auscultation revealed reduced respiratory sounds at both base, heart auscultation revealed a pericardial friction rub. Dermatologic examinations were normal. INVESTIGATIONS: Laboratory findings were notable for anemia, thrombopenia and leukocytosis, disseminated intravascular coagulation and markedly elevated CRP (309 mg/l). Electrogram showed inferior and lateral ST segment depression. Echocardiography showed pericardial effusion. Chest CT scan revealed bilateral pleural effusion, a left-sided small infiltrate and enlarged mediastinal lymph nodes. Abdominal ultrasound confirmed hepatosplenomegaly and ascites. TREATMENT AND CLINICAL COURSE: A diagnosis of parapneumonic bilateral pleural empyema, perimyocarditis and disseminated intravascular coagulation was made. Despite institution of empiric antibiotic therapy, no clinical improvement was observed. After exclusion of infectious, autoimmune or malignant disease, clinical and laboratory data, especially marked hyperferritinemia, helped to establish the diagnosis of adult-onset Still's disease. Immunosuppressive treatment with prednisolone and azathioprin resulted in remission. CONCLUSION: Adult-onset Still's disease is a rare inflammatory disorder of unknown origin, which may affect multiple organs. The diagnosis is based on a diagnostic score, which includes a number of clinical and laboratory findings, published by Yamaguchi in 1992. Marked hyperferritinemia represents an additional diagnostic clue to the disease.
DOI:doi:10.1055/s-2004-835297
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1055/s-2004-835297
 Volltext: http://www.thieme-connect.de/DOI/DOI?10.1055/s-2004-835297
 DOI: https://doi.org/10.1055/s-2004-835297
Datenträger:Online-Ressource
Sprache:ger
Sach-SW:Adult
 Azathioprine
 Disseminated Intravascular Coagulation
 Electrocardiography
 Empyema, Pleural
 Humans
 Immunosuppressive Agents
 Male
 Pericarditis
 Prednisolone
 Radiography, Thoracic
 Still's Disease, Adult-Onset
 Treatment Outcome
K10plus-PPN:180532117X
Verknüpfungen:→ Zeitschrift

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