Roberto Mogami1, João Luiz Pereira Vaz2, Yêdda de Fátima Barcelos Chagas3, Rodrigo Sperling Torezani4, André de Almeida Vieira4, Ana Célia Baptista Koifman1, Yasmin Baptista Barbosa5, Mirhelen Mendes de Abreu6. 1. PhD, Adjunct Professor of Radiology at the School of Medical Sciences of the Universidade do Estado do Rio de Janeiro (UERJ), Rio de Janeiro, RJ, Brazil. 2. PhD, Adjunct Professor of Rheumatology at the Universidade Federal do Estado do Rio de Janeiro (Unirio), Rio de Janeiro, RJ, Brazil. 3. MD, Resident in Rheumatology at the Hospital Universitário Gafrée e Guinle (HUGG) da Universidade Federal do Estado do Rio de Janeiro (Unirio), Rio de Janeiro, RJ, Brazil. 4. MD, Resident in Radiology at the Hospital Universitário Pedro Ernesto (HUPE) da Universidade do Estado do Rio de Janeiro (UERJ), Rio de Janeiro, RJ, Brazil. 5. Undergraduate Medical Student at the Universidade do Estado do Rio de Janeiro (UERJ), Rio de Janeiro, RJ, Brazil. 6. PhD, Adjunct Professor of Rheumatology at the Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brasil.
Abstract
OBJECTIVE: To describe the main ultrasound findings of chikungunya fever in the ankle. MATERIALS AND METHODS: This was a cross-sectional observational study involving 52 patients referred to the Hospital Universitário Pedro Ernesto and presenting with clinical and biochemical evidence of chikungunya fever. The examinations were performed by a radiologist with more than 20 years of experience in ultrasound. RESULTS: The predominant gender was female (in 88.5%), and the mean age was 58.4 years. The majority (61.5%) of the patients came from the northern part of the city of Rio de Janeiro, and 46.2% were using corticosteroids to treat inflammatory symptoms. The most common alterations observed by ultrasound were joint effusion (in 69.2%), tenosynovitis (in 59.6%), cellulitis (in 46.2%), Kager's fat pad thickening (in 29.9%), myositis (of the soleus or flexor hallucis longus muscle) (in 17.3%), retrocalcaneal bursitis (in 5.8%), tendon ruptures (in 3.8%), and increased vascular flow on power Doppler (in 3.8%). CONCLUSION: Signs of synovitis and tenosynovitis were the main ultrasound findings in a predominantly female population with a mean age of 58.4 years. Further studies are needed in order to define the role of ultrasound in the follow-up of such patients.
OBJECTIVE: To describe the main ultrasound findings of chikungunya fever in the ankle. MATERIALS AND METHODS: This was a cross-sectional observational study involving 52 patients referred to the Hospital Universitário Pedro Ernesto and presenting with clinical and biochemical evidence of chikungunya fever. The examinations were performed by a radiologist with more than 20 years of experience in ultrasound. RESULTS: The predominant gender was female (in 88.5%), and the mean age was 58.4 years. The majority (61.5%) of the patients came from the northern part of the city of Rio de Janeiro, and 46.2% were using corticosteroids to treat inflammatory symptoms. The most common alterations observed by ultrasound were joint effusion (in 69.2%), tenosynovitis (in 59.6%), cellulitis (in 46.2%), Kager's fat pad thickening (in 29.9%), myositis (of the soleus or flexor hallucis longus muscle) (in 17.3%), retrocalcaneal bursitis (in 5.8%), tendon ruptures (in 3.8%), and increased vascular flow on power Doppler (in 3.8%). CONCLUSION: Signs of synovitis and tenosynovitis were the main ultrasound findings in a predominantly female population with a mean age of 58.4 years. Further studies are needed in order to define the role of ultrasound in the follow-up of such patients.
Chikungunya fever is a disease caused by a virus of the family Togaviridae, genus
Alphavirus, transmitted by the mosquitoes Aedes
aegypti and Aedes albopictus(. Most infected patients become symptomatic, and the disease
progresses through three phases: an acute phase, which can last up to 10 days and is
characterized by fever, pain, periarticular edema, and, in many cases,
rash(; a subacute phase,
typically lasting from day 11 to month 3, in which rheumatic symptoms, characterized
by synovitis (of the large and small joints) and tenosynovitis, predominate; and a
chronic phase, beginning after the third month of evolution, in which there is
persistence of inflammatory symptoms at some sites, myalgia, and peripheral nerve
compressive syndromes. A small percentage of patients in the chronic phase develop
profiles resembling that of rheumatoid arthritis, and the main finding on imaging
studies is joint erosion(.The chikungunya virus was initially isolated in Tanzania in 1952. After sporadic
outbreaks of chikungunya fever in Africa and Asia throughout the 1960s and 1970s,
the disease became statistically significant following an epidemic in Kenya in 2004
and especially after the epidemic of the Reunion Islands (in the Indian Ocean) in
2005. The first cases in the Western Hemisphere occurred in the Caribbean in 2013,
and the virus spread to South American countries thereafter(.In Brazil, autochthonous cases were initially identified in 2014 in the municipality
of Oiapoque, located in the northern region of Brazil(. In 2015, there were 23,431 probable cases of
chikungunya fever in Brazil, which rose to 236,287 cases in 2016 (a 1,008.4%
increase), only up to the month of September. In 2016, the northeastern region
accounted for 88.2% of these cases and the southeastern region for accounted for
8.0%. Of the cases of chikungunya fever in the southeastern region in 2016, the city
of Rio de Janeiro accounted for 71.5%. The proportional increase in the number of
cases in 2016 (up through the October-November period) in the city of Rio de
Janeiro, in comparison with 2015, is even more absurd: 33,270%. That figure
corresponds to 0.2% of the population of the city, according to the 2010 census. If
we remember that in the Reunion Islands 30% of the population was affected by the
virus, we can have an idea of the magnitude of the problem in Brazil(.As a result of the outbreak in Rio de Janeiro, in the first half of 2016, emergency
rooms in the city were crowded with patients complaining of fever and severe
arthralgia. In a study published in a radiology journal, Mogami et al.( was the first to mention the Rio de
Janeiro outbreak and to describe the ultrasound alterations characteristic of
chikungunya fever. The present study continues that line of research. The main
objective was to describe the relevant changes that occur in the ankle as a result
of infection with the chikungunya virus.
MATERIALS AND METHODS
This was a cross-sectional observational study involving 52 patients referred to the
Radiology Department of Hospital Universitário Pedro Ernesto, in the city of
Rio de Janeiro, Brazil, between June and October of 2016. We included adult patients
(≥ 18 years of age), of either gender, with history of sudden-onset fever,
joint pain at multiple sites, with or without rash, and laboratory test results
indicating IgM/IgG positivity for a diagnosis of chikungunya fever. Patients with
rheumatic diseases such as rheumatoid arthritis, spondyloarthropathy, gout and
septic arthritis were excluded, as were those with sequelae of fractures. The study
was approved by the Research Ethics Committee of Hospital Universitário Pedro
Ernesto (Protocol no. 58066716.8.0000.5259). All participating patients gave written
informed consent.The ankle ultrasound examinations were performed by a radiologist with more than 20
years of experience in the method. In addition to the routine investigation of the
ankle, the same examiner evaluated the state of the calf muscles to identify any
signs suggestive of myositis. A total of 104 examinations were performed with an
ultrasound system (Aplio XG; Toshiba Medical Systems, Otawara, Japan), equipped with
a multifrequency linear transducer (14–18 MHz in Bmode) and with power Doppler.
RESULTS
Of the 52 patients in the sample, 6 (11.5%) were male and 46 (88.5%) were female. The
mean age was 58.4 years.The patients were stratified by their region of residence within the city, which was
divided into four main parts: 32 (61.5%) resided in the suburban, northern part of
the city; 10 (19.2%) resided in the western part; 9 (17, 3%) resided in the
periphery (within the greater metropolitan region) of the city, and only 1 (1.9%)
resided in the most exclusive, southern part of the city.The most common symptoms, in descending order, were joint pain, in 52 patients
(100%); fever, in 46 (88.5%); skin changes, in 37 (71.2%); pruritus, in 31 (59.6%);
paresthesias, in 22 (42.3%); and lymph node enlargement, in 4 (7.7%).At the time of the tests, 24 (46.2%) of the patients were using corticosteroids, 14
(26.9%) were taking no medication, 6 (11.5%) were using anti-inflammatory drugs, and
5 (9.6%) were using a combination of corticosteroids and immunosuppressants.On average, the ultrasound examinations were performed 4.1 months after the onset of
the disease, corresponding to the chronic phase.The most common ultrasound alterations in the ankles, in decreasing order of
frequency, were joint effusion (Figure 1), in
36 (69.2%) of the patients; tenosynovitis (Figure
2), in 31 (59.6%); cellulitis, in 24 (46.2%), thickening of Kager's fat
pad (Figure 3), in 14 (29.9%); myositis (of the
soleus muscle, flexor hallucis longus muscle, or both) (Figure 4), in 9 (17.3%); retrocalcaneal bursitis (Figure 5), in 3 (5.8%); tendon ruptures (Figure 6), in 2 (3.8%), and increased vascular
flow, as seen on power Doppler, in 2 (3.8%).
Figure 1
Longitudinal sagittal image of the tibiotarsal joint space, performed
with a linear transducer at 14 MHz, showing hypoechoic areas (arrows),
characteristic of effusion.
Figure 2
A: Photo of the dorsal region of the left foot, which shows
anterolateral bulging (arrows). B: Corresponding to the
alteration observed in the physical examination, ultrasound of the long
extensor tendon of the fingers, performed with a linear transducer at 14
MHz and acquired in the sagittal plane, shows distention of the tendon
sheath by an anechoic fluid collection (arrows), which is characteristic
of tenosynovitis.
Figure 3
Sagittal ultrasound image of the posterior calf region, performed with a
linear transducer at 14 MHz, showing thickening and increased
echogenicity of Kager's fat pad (arrows).
Figure 4
Sagittal panoramic view of the calf, performed by sweeping with a linear
transducer at 14 MHz, showing diffuse hyperechogenicity of the soleus
and flexor hallucis longus muscles, caused by myositis.
Figure 5
Sagittal image of the lower calf, performed with a linear transducer at
14 MHz, showing an anechoic fluid collection in the retrocalcaneal
bursal projection (arrow), which is characteristic of bursitis.
Figure 6
Cross-sectional image of the fibularis brevis muscle tendon, performed
with a linear transducer at 14 MHz, showing an extensive hypoechoic
area, indicative of a partial rupture, in the posterior region.
Longitudinal sagittal image of the tibiotarsal joint space, performed
with a linear transducer at 14 MHz, showing hypoechoic areas (arrows),
characteristic of effusion.A: Photo of the dorsal region of the left foot, which shows
anterolateral bulging (arrows). B: Corresponding to the
alteration observed in the physical examination, ultrasound of the long
extensor tendon of the fingers, performed with a linear transducer at 14
MHz and acquired in the sagittal plane, shows distention of the tendon
sheath by an anechoic fluid collection (arrows), which is characteristic
of tenosynovitis.Sagittal ultrasound image of the posterior calf region, performed with a
linear transducer at 14 MHz, showing thickening and increased
echogenicity of Kager's fat pad (arrows).Sagittal panoramic view of the calf, performed by sweeping with a linear
transducer at 14 MHz, showing diffuse hyperechogenicity of the soleus
and flexor hallucis longus muscles, caused by myositis.Sagittal image of the lower calf, performed with a linear transducer at
14 MHz, showing an anechoic fluid collection in the retrocalcaneal
bursal projection (arrow), which is characteristic of bursitis.Cross-sectional image of the fibularis brevis muscle tendon, performed
with a linear transducer at 14 MHz, showing an extensive hypoechoic
area, indicative of a partial rupture, in the posterior region.Fluid collections were located in the tibiotarsal joint space (Figure 1) in 27 (51.9%) patients and in the proximal intertarsal
joint space in 23 (44.2%). Signs of tenosynovitis were found mainly in the posterior
tibial sheath and fibular sheath-in 19 (36.5%) and 17 (32.7%) of the patients,
respectively.Pre-existing calcaneal tendon lesions were noted: calcifications were observed in 33
(63.5%) of the patients, and tendinopathy was observed in 6 (11.5%). In 13 patients
(25%), there were no Achilles tendon lesions.
DISCUSSION
The use of imaging examinations in the investigation of infections, especially those
of regional incidence, have been the subject of various studies in the radiology
literature of Brazil(. This paper presents the partial
results of a larger, ongoing study at Rio de Janeiro State University, which is
investigating musculoskeletal involvement of the upper and lower limbs in
individuals with chikungunya fever. The studied population presented in the subacute
or chronic phases of the disease, as can be seen by the mean time elapsed between
the diagnosis and the performance of the examinations (4.1 months). There was a
marked predominance of females, as well as of individuals in a higher age group
(mean age, 58.4 years). These findings are similar to those of a study conducted on
the island of Martinique( and
of the classic work on the chikungunya fever epidemic in the Reunion
Islands( but quite
different from those of studies conducted in India(, Italy(, Sri Lanka(, and Colombia(. In the literature, it has been demonstrated that chikungunya
fever patients over 35 years of age have an increased risk of developing chronic
arthralgia(.The fact that the majority of cases studied were in residents of the northern,
suburban part of the city could be indicative of the vulnerability of that region to
mosquito proliferation. However, it might also represent a geographical bias, due to
the location of the hospital at which the study was located. However, data from the
Rio de Janeiro Municipal Health Department show that during April of 2016, when the
monthly number of reported cases of chikungunya fever was highest (5,109), the most
affected neighborhoods were located in the northern and western parts of the
city(.All of the symptoms reported have been described in the literature as being
associated with arbovirus infections, and chronic joint pain has been specifically
associated with chikungunya(.The heterogeneity of practices in relation to the treatment of patients reflects the
lack of knowledge about the disease and the flow of patients referred from general
or specialized outpatient clinics, as well as from emergency rooms in Rio de
Janeiro.Consistent with the literature, in our study, ankle involvement occurred
symmetrically(. The two main alterations were effusion and tenosynovitis,
as in other anatomical segments(. In the chronic phase of the disease, these collections
are not very voluminous, although most, especially tenosynovitis, respond well to
anti-inflammatory treatment. In the follow-up examinations, we observed cases in
which there was regression of the inflammatory condition but persistence of residual
asymmetric intra- or extra-articular foci, which merit additional study in order to
identify any associated joint erosion.Myositis, with or without cellulitis, was identified in 17.3% of the patients. The
muscles most often affected in our sample were the soleus and flexor hallucis
longus. Frequently, there was associated involvement of Kager's fat pad, which was
hyperechoic and formed a continuous ultrasound aspect similar to that of myositis of
the soleus muscle. The involvement is almost always symmetrical, and in the case of
the lower limbs it is associated with complaints of fatigue and discomfort in the
calf region. We believe that the bent position that gave rise to the name
"chikungunya" in the Makonde dialect of Tanzania( relates not only to ankle arthritis but also to
generalized myositis of the sural musculature. In follow-up examinations, we found
that myositis can persist for a long time, even when the patient responds well to
steroid and immunosuppressive therapy. Because viral agents can cause idiopathic
inflammatory myopathies, infection with the chikungunya virus might also trigger
this type of condition in the long term(. Inflammatory involvement secondary to infection is a
subject that has been discussed for some time, and the chikungunya virus has been
associated with such involvement(.In the present study, power Doppler showed inflammation in 3.8% of the ankles
evaluated, as has been reported for the hands and wrists, albeit at an even lower
frequency (Mogami, unpublished data). We believe that the greatest utility of this
resource is in the follow-up of patients. Increased vascular flow in follow-up
examinations might signal persistent inflammatory foci and alert the attending
physician to the possibility of chronic inflammatory rheumatism(. That hypothesis should be tested in further studies.One musculoskeletal comorbidity found in chikungunya fever patients was the
involvement of the calcaneal tendon, either by enthesopathy (in 63.5%) or by
tendinopathy (in 11.5%). In practice, this translates to amplification of symptoms
existing prior to infection with the virus. Complaints of pain intensification are
common during the chronic phase of the disease. Chen et al.( stated that pre-existing
degenerative musculoskeletal diseases could prolong the symptoms of arthralgia.
Therefore, such comorbidities are of clinical relevance in the follow-up of these
patients.After the outbreak of chikungunya fever in 2016(, the expectation of the Brazilian health
authorities is that the disease will return more forcefully in the summer of 2017.
Despite the limitations of this study, the characterization and pioneering
quantification of ankle lesions by ultrasound was an important means of highlighting
the role that the method plays in the diagnosis of such complications. Additional
studies are needed in order to evaluate the role that ultrasound plays in the
monitoring individuals infected with the chikungunya virus and in the identification
of cases that might progress to chronic inflammatory rheumatism or even secondary
rheumatoid arthritis(. This
need for follow-up studies of cases of chronic arthralgia with the potential for
developing inflammatory arthritis has been cited by other authors(.In summary, the 2015–2016 epidemic outbreak in Rio de Janeiro was characterized by
the predominant involvement of older women who lived in the suburbs and by the lack
of a clearly defined treatment for disease, most of them on steroids. The
predominant findings in our series were effusion and tenosynovitis, mainly fibular
and posterior tibial. The most common musculoskeletal comorbidity was involvement of
the calcaneal tendon. Power Doppler was not very useful in the identification of
areas with synovial inflammation.
Authors: Simon-Djamel Thiberville; Nanikaly Moyen; Laurence Dupuis-Maguiraga; Antoine Nougairede; Ernest A Gould; Pierre Roques; Xavier de Lamballerie Journal: Antiviral Res Date: 2013-06-28 Impact factor: 5.970