Muskuläre Sarkozystose nach Malaysiareise: eine Fallserie aus Deutschland

Standard

Muskuläre Sarkozystose nach Malaysiareise: eine Fallserie aus Deutschland. / Slesak, G; Tappe, D; Keller, Christian; Cramer, J; Güthoff, W; Zanger, P; Frank, M; Ernestus, K; Rauthe, S; Stich, A; Schäfer, J.

In: DEUT MED WOCHENSCHR, Vol. 139, No. 19, 01.05.2014, p. 990-5.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Slesak, G, Tappe, D, Keller, C, Cramer, J, Güthoff, W, Zanger, P, Frank, M, Ernestus, K, Rauthe, S, Stich, A & Schäfer, J 2014, 'Muskuläre Sarkozystose nach Malaysiareise: eine Fallserie aus Deutschland', DEUT MED WOCHENSCHR, vol. 139, no. 19, pp. 990-5. https://doi.org/10.1055/s-0034-1370004

APA

Slesak, G., Tappe, D., Keller, C., Cramer, J., Güthoff, W., Zanger, P., Frank, M., Ernestus, K., Rauthe, S., Stich, A., & Schäfer, J. (2014). Muskuläre Sarkozystose nach Malaysiareise: eine Fallserie aus Deutschland. DEUT MED WOCHENSCHR, 139(19), 990-5. https://doi.org/10.1055/s-0034-1370004

Vancouver

Slesak G, Tappe D, Keller C, Cramer J, Güthoff W, Zanger P et al. Muskuläre Sarkozystose nach Malaysiareise: eine Fallserie aus Deutschland. DEUT MED WOCHENSCHR. 2014 May 1;139(19):990-5. https://doi.org/10.1055/s-0034-1370004

Bibtex

@article{2cd93162dda64b58a5aacb3a8169d025,
title = "Muskul{\"a}re Sarkozystose nach Malaysiareise: eine Fallserie aus Deutschland",
abstract = "BACKGROUND: Since 2011, about 100 travellers to the island of Tioman, Malaysia, have been diagnosed worldwide with suspected muscular sarcocystosis, a previously only sporadically observed parasitic disease. Source of infection and therapy remain unclear. Final diagnosis requires microscopic identification of cysts in muscle biopsies. The study objective was a systematic description of characteristic symptoms, laboratory investigations and treatment response.METHODS: Systematic case series.RESULTS: The 26 cases of 5 centers for tropical medicine in Germany showed a characteristic biphasic development: symptoms began in general 2 weeks after mid-holidays (min. 7.5, max. 22 days) with unspecific fever and headaches lasting for almost 1 week. After an asymptomatic period of 2 weeks, severe myalgia (6.5, scale 0-10) and fever developed and lasted for about 6 weeks (min. 7, max. 207 days), accompanied by creatin-phosphokinase(CK)-elevation (up to 3.5 times), and eosinophilia (2.9 times). One out of two muscle biopsies revealed a cyst typical for sarcocystosis. In 6 out of 7 patients an increase in Sarcocystis-specific antibody concentration could be demonstrated by ELISA. Treatment with systemic steroids and albendazole, or ivermectin resulted in significant symptomatic improvement in most of the patients. One patient was treated early with cotrimoxazole and subsequently did not develop a second phase of the disease. All patients had stayed in the North-West of the island Tioman.CONCLUSIONS: Muscular sarcocystosis develops in a biphasic pattern with initial fever and later prolonged myalgia, eosinophilia, and CK-elevation. Steroids achieve symptomatic relief in the late phase. Early cotrimoxazole-therapy could possibly prevent parasitic muscle invasion. In fever after travel to Malaysia differential diagnosis should include sarcocystosis. The source of infection appears to be located in North-West of Tioman. Further studies are needed, including addressing early diagnosis and treatment.",
keywords = "Adolescent, Adult, Antibodies, Protozoan, Biopsy, Child, Developing Countries, Diagnosis, Differential, Enzyme-Linked Immunosorbent Assay, Female, Fever of Unknown Origin, Germany, Humans, Infectious Disease Incubation Period, Malaysia, Male, Middle Aged, Muscle, Skeletal, Myalgia, Sarcocystis, Sarcocystosis, Travel, Young Adult",
author = "G Slesak and D Tappe and Christian Keller and J Cramer and W G{\"u}thoff and P Zanger and M Frank and K Ernestus and S Rauthe and A Stich and J Sch{\"a}fer",
note = "{\textcopyright} Georg Thieme Verlag KG Stuttgart · New York.",
year = "2014",
month = may,
day = "1",
doi = "10.1055/s-0034-1370004",
language = "Deutsch",
volume = "139",
pages = "990--5",
journal = "DEUT MED WOCHENSCHR",
issn = "0012-0472",
publisher = "Georg Thieme Verlag KG",
number = "19",

}

RIS

TY - JOUR

T1 - Muskuläre Sarkozystose nach Malaysiareise: eine Fallserie aus Deutschland

AU - Slesak, G

AU - Tappe, D

AU - Keller, Christian

AU - Cramer, J

AU - Güthoff, W

AU - Zanger, P

AU - Frank, M

AU - Ernestus, K

AU - Rauthe, S

AU - Stich, A

AU - Schäfer, J

N1 - © Georg Thieme Verlag KG Stuttgart · New York.

PY - 2014/5/1

Y1 - 2014/5/1

N2 - BACKGROUND: Since 2011, about 100 travellers to the island of Tioman, Malaysia, have been diagnosed worldwide with suspected muscular sarcocystosis, a previously only sporadically observed parasitic disease. Source of infection and therapy remain unclear. Final diagnosis requires microscopic identification of cysts in muscle biopsies. The study objective was a systematic description of characteristic symptoms, laboratory investigations and treatment response.METHODS: Systematic case series.RESULTS: The 26 cases of 5 centers for tropical medicine in Germany showed a characteristic biphasic development: symptoms began in general 2 weeks after mid-holidays (min. 7.5, max. 22 days) with unspecific fever and headaches lasting for almost 1 week. After an asymptomatic period of 2 weeks, severe myalgia (6.5, scale 0-10) and fever developed and lasted for about 6 weeks (min. 7, max. 207 days), accompanied by creatin-phosphokinase(CK)-elevation (up to 3.5 times), and eosinophilia (2.9 times). One out of two muscle biopsies revealed a cyst typical for sarcocystosis. In 6 out of 7 patients an increase in Sarcocystis-specific antibody concentration could be demonstrated by ELISA. Treatment with systemic steroids and albendazole, or ivermectin resulted in significant symptomatic improvement in most of the patients. One patient was treated early with cotrimoxazole and subsequently did not develop a second phase of the disease. All patients had stayed in the North-West of the island Tioman.CONCLUSIONS: Muscular sarcocystosis develops in a biphasic pattern with initial fever and later prolonged myalgia, eosinophilia, and CK-elevation. Steroids achieve symptomatic relief in the late phase. Early cotrimoxazole-therapy could possibly prevent parasitic muscle invasion. In fever after travel to Malaysia differential diagnosis should include sarcocystosis. The source of infection appears to be located in North-West of Tioman. Further studies are needed, including addressing early diagnosis and treatment.

AB - BACKGROUND: Since 2011, about 100 travellers to the island of Tioman, Malaysia, have been diagnosed worldwide with suspected muscular sarcocystosis, a previously only sporadically observed parasitic disease. Source of infection and therapy remain unclear. Final diagnosis requires microscopic identification of cysts in muscle biopsies. The study objective was a systematic description of characteristic symptoms, laboratory investigations and treatment response.METHODS: Systematic case series.RESULTS: The 26 cases of 5 centers for tropical medicine in Germany showed a characteristic biphasic development: symptoms began in general 2 weeks after mid-holidays (min. 7.5, max. 22 days) with unspecific fever and headaches lasting for almost 1 week. After an asymptomatic period of 2 weeks, severe myalgia (6.5, scale 0-10) and fever developed and lasted for about 6 weeks (min. 7, max. 207 days), accompanied by creatin-phosphokinase(CK)-elevation (up to 3.5 times), and eosinophilia (2.9 times). One out of two muscle biopsies revealed a cyst typical for sarcocystosis. In 6 out of 7 patients an increase in Sarcocystis-specific antibody concentration could be demonstrated by ELISA. Treatment with systemic steroids and albendazole, or ivermectin resulted in significant symptomatic improvement in most of the patients. One patient was treated early with cotrimoxazole and subsequently did not develop a second phase of the disease. All patients had stayed in the North-West of the island Tioman.CONCLUSIONS: Muscular sarcocystosis develops in a biphasic pattern with initial fever and later prolonged myalgia, eosinophilia, and CK-elevation. Steroids achieve symptomatic relief in the late phase. Early cotrimoxazole-therapy could possibly prevent parasitic muscle invasion. In fever after travel to Malaysia differential diagnosis should include sarcocystosis. The source of infection appears to be located in North-West of Tioman. Further studies are needed, including addressing early diagnosis and treatment.

KW - Adolescent

KW - Adult

KW - Antibodies, Protozoan

KW - Biopsy

KW - Child

KW - Developing Countries

KW - Diagnosis, Differential

KW - Enzyme-Linked Immunosorbent Assay

KW - Female

KW - Fever of Unknown Origin

KW - Germany

KW - Humans

KW - Infectious Disease Incubation Period

KW - Malaysia

KW - Male

KW - Middle Aged

KW - Muscle, Skeletal

KW - Myalgia

KW - Sarcocystis

KW - Sarcocystosis

KW - Travel

KW - Young Adult

U2 - 10.1055/s-0034-1370004

DO - 10.1055/s-0034-1370004

M3 - SCORING: Zeitschriftenaufsatz

C2 - 24782151

VL - 139

SP - 990

EP - 995

JO - DEUT MED WOCHENSCHR

JF - DEUT MED WOCHENSCHR

SN - 0012-0472

IS - 19

ER -