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Medicina Clínica (English Edition) Q fever spondylitis: 2 cases report
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Vol. 153. Issue 1.
Pages 41-42 (July 2019)
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Q fever spondylitis: 2 cases report
Espondilodiscitis por fiebre Q. Descripción de 2 casos
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Neus Muñoza,
Corresponding author
neus85@gmail.com

Corresponding author.
, Bárbara Gonzálezb, Bernat Fontc
a Departamento de Medicina Interna, Corporació Hospital Parc Taulí de Sabadell, Sabadell, Barcelona, Spain
b Departamento de Geriatría, Corporació Hospital Parc Taulí de Sabadell, Sabadell, Barcelona, Spain
c Departamento d Enfermedades Infecciosas, Corporació Hospital Parc Taulí de Sabadell, Sabadell, Barcelona, Spain
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Q fever is a zoonosis caused by Coxiella burnetii. This microorganism is an intracellular bacterium and causes acute and chronic infections. The most common manifestations of this entity include endocarditis, chronic vascular and osteoarticular infections.

The diagnosis is based on histological examinations, serology and/or PCR in cell cultures.1–4

Spondylitis caused by C. burnetii (Q fever) is a rare entity, with few cases reported to date. Therefore, we believe it is of interest to describe the cases of 2 patients assisted in our center with this diagnosis.

Case 1

A 49-year-old man with no significant history, suffering from lumbosacral pain for 2 weeks, without fever or any other symptoms. Normal physical examination except for lower back pain on palpation. Blood test with normal complete blood count, liver and kidney biochemistry, ESR and PCR. Normal chest X-ray. Blood cultures, PPD and Quantiferon® were negative. In lumbar MRI, signs of L3–L4 spondylodiscitis with peri-vertebral abscesses and abscesses in the left psoas muscle and left anterior intraspinal-epidural abscess (L3–L4 and L4–L5) (Fig. 1). Pathological anatomy with signs of chronic granulomatous inflammation and multinucleated giant cells. Kinyoun, Gram, Ziehl–Neelsen staining, Lowenstein and PCR negative for mycobacteria. Brucella, Bartonella serologies and Rose Bengal were negative. Serology for C. burnetii was positive (Coxiella IgG positive phase I 2560; phase II 1/640, IgA phase I 1/800, phase II 1/25). Normal echocardiogram and visceral arterial Doppler ultrasonography. With the diagnosis of Q fever spondylodiscitis, the therapy used was hydroxychloroquine 200mg/12h, doxycycline 100mg/12h and rifampicin 600mg/24h for 2 years. Subsequently, the therapy was changed to doxycycline with levofloxacin 750mg/24h for 3 years until negative serology.

Fig. 1.

Lumbar MRI of cases 1 and 2.

During the follow-up, the patient presented good clinical and radiological evolution. In a control MRI in 2010, improvement of peri-vertebral abscesses. In the 2012 control MRI: residual changes in the L3–L4 intervertebral disc space in relation to the old spondylodiscitis without edematous-inflammatory signs at the vertebral bodies.

Case 2

A 59-year-old woman with a history of osteoarthritis and dorsalgia for 4 years of controlled evolution with analgesia. She consulted for back pain worsening, that led to a significant functional impairment, without fever or any other accompanying symptoms. A physical examination highlighted selective pain to palpation of Th7–Th8 vertebrae, the rest being anodyne. Blood test with normal complete blood count, liver and kidney biochemistry, ESR and PCR. Normal chest X-ray. Blood cultures, PPD and Quantiferon were negative. In the bone scintigraphy, signs of spondylodiscitis in Th8–Th9; and in thoracic MRI with ankylosing spondylitis of the Th8–Th9 mid-thoracic segment and spondylodiscitis and right Th6-Th7 vertebral arthritis without involvement of the spinal canal (Fig. 1).

Biopsy with microbiological study (Gram, Ziehl–Neelsen staining, bacteria culture, Lowenstein and PCR for mycobacteria) showed a negative result. The pathological anatomy was not conclusive (insufficient specimen) and the patient refused to undergo a new puncture. Brucella and Bartonella serologies and Rose Bengal test were negative. Serology for C. burnetii was positive (Anti-Coxiella IgG phase I 1/1280, phase II 1/640, IgA phase I 1/400, phase II 1/50, IgM phase I negative, phase II 1/50). Normal echocardiogram. The patient underwent 9 months of tuberculostatic therapy and doxycycline 100mg/12h, subsequently maintaining doxycycline 100mg/2h and rifampicin 600mg/12h along with hydroxychloroquine 200mg/12h for 2 years. Subsequently, when serology improved, therapy was changed to doxycycline and levofloxacin 750mg/24h. After 4 years of evolution, the patient presented clinical and radiological improvement. Control MRI at year 2 shows improvement of edema from Th4 toTh10 predominant in Th5.

Although spondylitis due to Q fever is a rare entity in our setting, it should be considered in the differential diagnosis of infectious spondylitis. In the bibliography, there are only 20–30 reported cases.

And, to a greater extent, in patients with subacute forms of presentation, where the pathological anatomy shows granulomatous lesions and the diagnosis of tuberculosis has not been verified. The best methods of microbiological diagnosis are those that allow direct detection of the bacteria (cell culture and polymerase chain reaction, PCR). Indirect immunofluorescence is very sensitive and specific. These diagnostic methods should also be associated with antibody titers (IgG and/or IgM), higher than the cut-off point.

Since it requires antibiotic therapy for months, the patient should undergo clinical, radiological and serological follow-up. The decrease of over 2 antibody titers is considered a good evolution. To consider healing, we require IgG <1:400 and negative IgA, in this case the treatment could be withdrawn.5

References
[1]
M. Etienne, S. Simon, E. Antoine, C. Etienne, R. Blandine, M. Matthieu, et al.
Osteoarticular manifestations of Q fever: a case series and literature review.
Clin Microbiol Infect, 30 (2018), pp. 211-218
[2]
D. Raoult, T. Marrie, J. Mege.
Natural history and pathophysiology of Q fever.
Lancet Infect Dis, 5 (2005), pp. 219-226
[3]
V. Merhej, P. Tattevin, M. Revest, B. Le Touvet, D. Raoult.
Q fever osteomyelitis: a case report and literature review.
Comp Microbiol Infect Dis, 35 (2012), pp. 169-172
[4]
L.M. Kampschreur, M.C. Wegdam-Blans, P.C. Wever, N.H. Renders, C.E. Delsing, T. Sprong, Dutch Q Fever Consensus Group, et al.
Chronic Q fever diagnosis – consensus guideline versus expert opinion.
Group Emerg Infect Dis, 21 (2015), pp. 1183-1188
[5]
S. Sunder, G. Gras, F. Bastides, C. de Gialluly, P. Choutet, L. Bernard.
Chronic Q fever: relevance of serology.
Clin Infect Dis, 53 (2011), pp. 749-750

Please cite this article as: Muñoz N, González B, Font B. Espondilodiscitis por fiebre Q. Descripción de 2 casos. Med Clin (Barc). 2019;153:41–42.

Copyright © 2018. Elsevier España, S.L.U.. All rights reserved
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