ARTICLE
Auteur(s) : Melih
AKYOL1, Sedat ÖZÇELIK1, Aynur
ENGIN2, Sibel Berksoy HAYTA1, Fatma
BIÇICI1
1Dermatology Department, Cumhuriyet University,
School of Medicine, 58140 Sivas, Turkey
2Clinical Microbiology Department, Cumhuriyet
University, School of Medicine, 58140 Sivas, Turkey
Crimean-Congo Haemorrhagic Fever (CCHF) is a zoonotic viral
disease that is asymptomatic in infected animals. This virus is a
member of the genus Nairovirus in the family Bunyaviridae. CCHF is
widespread in Africa, the Middle East and Asia. CCHF has increased
in the last five years in Turkey and it is emerging as a public
health problem [1, 2]. The aim of this study was to reveal viral
morbilliform eruptions and other cutaneous manifestations of
CCHF.
The study group consisted of 35 patients who presented at
the hospital between June and July 2009. Acute and convalescent
phase serum samples were sent to the Virology Laboratory of Refik
Saydam Hygiene Central Institute, Ankara, Turkey for serologic and
virologic analyses. The definitive diagnosis of CCHF infection was
based upon typical clinical and epidemiological findings and
detection of CCHF virus-specific IgM by ELISA, or of genomic
segments of the CCHF virus by reverse transcription-polymerase
chain reaction (RT-PCR), in either the acute or convalescent phase
of the disease. The patients were examined by two experienced
dermatologists and the cutaneous manifestations were noted.
Laboratory analyses, including complete blood count, platelet
count, liver function tests, urine analysis, prothrombin time (PT),
activated partial thromboplastin time (aPTT) were evaluated in all
patients. Seventeen patients received ribavirin treatment. All the
patients in our study recovered without complications.
The mean age of the patients was 55.05 (range = 16-88, SD =
18.2). There were 26 (74.3%) males and 9 (25.7%) females.
Twenty six (74.3%) patients had a history of a tick bite or
contact. Bite marks could not be found in eight patients. Twenty
nine patients (82.9%) lived in rural areas whereas 6 (17.1%)
were in cities.
In our study, of the 35 patients with CCHF, 30 (83.3%)
had associated mucocutaneous manifestations (table 1). Five patients (14.3%) had pruritus. The
lips of five patients (14.3%) showed hemorrhagic crusting. Two
patients (5.7%) had erythematous and crusting tongues.
Table 1 Mucocutaneous lesions and proportional
distribution
|
Lesion types
|
N
|
%
|
|
Petechia/purpura
|
20
|
57.1
|
|
Ecchimosis
|
23
|
65.7
|
|
Morbiliform
|
11
|
31.4
|
|
Oral erythema/petechia
|
12
|
34.2
|
|
Conjunctival erythema
|
5
|
14.3
|
The anatomical regions in which the lesions were most frequently
seen were: upper extremities (62.9%), lower extremities (34.3%),
posterior trunk (28.6%), head-neck (28.6%) and anterior trunk
(25.7%).
The mean disease duration was 5.85 ± 2.78 days at the time
of examination. All the patients had a thrombocytopenia. The mean
value of platelet counts was 49,057.14 per mm3
(min-max: 6,000-98,000). Patients were divided into two groups
according to the number of platelets. Morbilliform eruption was
more frequently seen in patients with less than
50,000 platelets per mm3 of blood (p = 0.03,
χ2 = 4.29; Fisher exact test). Pearson correlation
analysis was used to determine the relation between platelet count
and having morbilliform eruption. A statistically significant
moderate correlation between both parameters was found (p = 0.01, r
= – 0.41). There was no relation between the morbilliform
eruption and the use of ribavirin (p = 0.33, χ2 =
0.93; Fisher exact test).
The most common skin findings of CCHF were petechia, purpura,
and ecchimosis, consistent with the pathogenesis of the disorder.
The anatomical regions where the lesions are mostly seen are the
extremities, which are more liable to trauma. In two patients
showing generalized lesions, platelet counts were 35,000 per
mm3 and 28,000 per mm3.
Erythematous and petechial eruptions may be seen in patients
with CCHF. Simple exanthems are erythematous changes in the skin
without evidence of blistering or pustulation in typical
morbilliform eruptions. The eruption typically starts on the trunk
and spreads peripherally in a symmetrical manner, and may be
maintained locally or become generalized. The most frequent
differential diagnosis in these patients is drug eruption [3].
Morbilliform eruption was not significantly more frequently seen in
our patients with ribavirin treatment. Therefore, in our study,
morbilliform eruption, which was detected more frequently in
patients with low platelet counts (< 50,000 per
mm3), may be considered as a viral toxidermic reaction.
Platelet count was below 20,000 per mm3 in only one
of eleven patients with a morbilliform eruption in our study.
Platelet count below 20,000 per mm3 is a prognostic
factor in terms of fatal outcome according to Swanepoel criteria
[4]. Consequently, morbilliform eruptions should be considered as
viral toxidermic reactions rather than being a predictive factor
for fatal outcome during the course of the disease.
CCHF is a viral disease causing mostly non-specific cutaneous
manifestations, including petecchia/purpura, and ecchimosis.
However, it should be kept in mind that morbilliform eruptions may
be a sign of a reduced number of platelets in cases of CCHF.
Acknowledgements
The authors thank Refik Saydam Hygiene Center of Ankara, Turkey for
testing the serum samples and our colleagues from the Turkish
Ministry of Health for their contributions. Financial support:
none. Conflict of interest: none.
References
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