gms | German Medical Science

87. Jahresversammlung der Deutschen Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie e. V.

Deutsche Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie e. V.

04.05. - 07.05.2016, Düsseldorf

The special case of a young adult with a life-threatening complication of an oropharyngeal infection

Meeting Abstract

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German Society of Oto-Rhino-Laryngology, Head and Neck Surgery. 87th Annual Meeting of the German Society of Oto-Rhino-Laryngology, Head and Neck Surgery. Düsseldorf, 04.-07.05.2016. Düsseldorf: German Medical Science GMS Publishing House; 2016. Doc16hno09

doi: 10.3205/16hno09, urn:nbn:de:0183-16hno091

Veröffentlicht: 7. September 2016

© 2016 Hartmann et al.
Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung). Lizenz-Angaben siehe http://creativecommons.org/licenses/by/4.0/.


Gliederung

Text

Introduction: Oropharyngeal infections with complication like a peritonsillar abszess are a typical clinical case in the daily practice of an otorhinolaryngologist. Rarely they appear in combinations with hereditary predisposition. We want to present one of these cases.

Case: The patient applied to our clinic with temperature at 44°C with acute thoracic ache provoked by respiration. She has had sore throat during the last week. In the examination there was especially no sign of a PTA. In labatory tests a leukopenia (2.3 Gpt/l) and thrombocytopenia (48 Gpt/l) were dectected. The PCT was at 98.7 ng/ml.

Because of the difference between the clinical picture and the diagnostic findings we decided to undertake a computer tomography of the neck/throat/abdomen.

A PTA in the left tonsil was visible on the scale of 8mm, also a jugular vein thrombosis and multiple septic emboli were detected. We conducted a tonsillectomy.

Furthermore we initated and calculated antbiosis and a full dose heparinization. Blood culture exposed Fusobacterium necrophorum and staphylococcus warnei.

We assumed a thrombotic predisposition because of the decribed clinical constellation. There appeared a positive family history and clinical proof in labatory test on our patient for Protein-C-deficit. Therefore a thrombophilia was detected.

Discussion: The synopsis of all diagnostic findings in our case is conformable to the lemierre-syndrom. The incidence rate of lemierre-syndrom is 14.4/1 Mio at the age of 15–24 years [1]. Only few cases demonstrate a connection between lemierre-syndrom and thrombophilia. To date a deficit of factor V [2] and other rare genetic changes in the coagulation system are proved [3]. In our case there was a labatory confirmed Protein-C deficit. Protein-C is a protease and a lack of it lead to a thrombophilia. Additional she took a contraceptive pill.

Conclusion: We concluded that a interference in the coagulation system has to be eliminated when there is a young person with discrepancy of local clinical findings and a servere clinical picture.


References

1.
Hagelskjaer Kristensen L, Prag J. Lemierre’s syndrome and other disseminated Fusobacterium necrophorum infections in Denmark: a prospective epidemiological and clinical survey. Eur J Clin Microbiol Infekt Dis. 2008 Sep;27(9):779-89.
2.
Lakshminarayana PH, Woodske ME. A unique case of lemierre syndrome associated with thrombophilia in an adult and the role of anticoagulation. Case Rep Med. 2010;2010. pii: 982494.
3.
Constantin JM, Mira JP, Guerin R, Cayot-Constatin S, Lesens O, Gourdon F, Romaszko JP, Linval P, Laurchesse H, Bazin JE. Lemierre’s syndrome and genetic polymorphisms: a case report. BMC Infect Dis. 2006 Jul 17;6:115.