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CASE REPORT
Year : 2014  |  Volume : 31  |  Issue : 4  |  Page : 401-403  

Endobronchial ultrasound guided needle aspiration of a paraspinal mass with prior failed multiple diagnostic interventions: A case report and literature review


1 Department of Pulmonary Medicine, Fortis Hospitals, Bengaluru, Karnataka, India
2 Department of Pathology, Fortis Hospitals, Bengaluru, Karnataka, India
3 Department of Neurosurgry, Fortis Hospitals, Bengaluru, Karnataka, India
4 Department of Radiology, Fortis Hospitals, Bengaluru, Karnataka, India

Date of Web Publication1-Oct-2014

Correspondence Address:
Dr. Nishant Sinha
Fortis Hospitals, 154/9, Banerghatta Road, Opposite IIM B, Bengaluru - 560 076, Karnataka
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0970-2113.142149

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   Abstract 

The increasing frequency of tuberculosis (TB) in both developed and developing countries has continued to make spinal TB an important health problem. The present case report is about a patient who presented to us with progressive back pain and paraspinal mass. We performed endobronchial ultrasound guided needle aspiration from the paraspinal mass. The cytology showed granulomatous inflammation suggestive of TB.

Keywords: Endobronchial ultrasound, paraspinal mass, transbronchial needle aspiration


How to cite this article:
Sinha N, Padegal V, Jermely D, Satyanarayana S, Santosh H K. Endobronchial ultrasound guided needle aspiration of a paraspinal mass with prior failed multiple diagnostic interventions: A case report and literature review. Lung India 2014;31:401-3

How to cite this URL:
Sinha N, Padegal V, Jermely D, Satyanarayana S, Santosh H K. Endobronchial ultrasound guided needle aspiration of a paraspinal mass with prior failed multiple diagnostic interventions: A case report and literature review. Lung India [serial online] 2014 [cited 2019 Nov 14];31:401-3. Available from: http://www.lungindia.com/text.asp?2014/31/4/401/142149


   Introduction Top


Spinal involvement occurs in less than 1% of patients with tuberculosis (TB). [1],[2],[3] Linear probe endobronchial ultrasound (EBUS), with the ability to perform real-time transbronchial needle aspiration (EBUS-TBNA), has increased the diagnostic possibilities for mediastinal and hilar lymphadenopathy, including lymph nodes metastasis of lung cancer, sarcoidosis, tuberculous lymphadenopathy, and lymphoma. However, there is limited experience on usefulness of EBUS-TBNA in the diagnosis of non-lymph node lesions like tubercular involvement of thoracic spine.


   Case Report Top


This was a case report of a 65-year-old gentleman who was admitted in the neurosurgery ward with gradually progressive back ache for 3 month. He had no history of cough, fever, loss of weight or appetite. Routine blood examinations were normal. Neurological examination, bowel and bladder functions were normal. Systemic examination was normal. Serum protein electrophoresis was normal. Skin test for Mycobacterium tuberculosis (Purified Protein Derivative with 5 TU) was negative. Serum Brucella titer was negative and he was seronegative for human immunodeficiency virus. There was no other significant medical illness. He was earlier treated empirically with anti-tuberculosis (TB) medications for 2 weeks, which the patient has stopped prior to coming to us.

Contrast enhanced magnetic resonance imaging (MRI) of dorsal spine showed predominantly enhancing soft-tissue swelling in the pre/para-vertebral and anterior epidural aspect of the spinal canal at T6-T7 level causing thecal sac compression. It extended superiorly up to T4 vertebral level and inferiorly until T8 vertebral level. There was no spinal instability or cord compression requiring any urgent neurosurgical intervention.

Computed tomography (CT) guided fine needle aspiration cytology (FNAC) was done from the posterior approach and cytology showed only degenerated cells and no definite comment could be made by the pathologist. CT guided tru-cut biopsy through the posterior approach to the right side of T7-T8 spine showed fibro adipose tissue, focal lymphoid aggregates, which were partially crushed. There were no definite granulomas or malignant cells. Bone marrow aspirate and bone biopsy of T7-T8 spine did not show granulomas, acid fast bacilli (AFB) or malignant cells. Second CT guided tru-cut biopsy also could not yield a diagnosis.

Subsequently rigid pleuroscopy guided biopsy was done from paravertebral tissue and mediastinal pleura under general anesthesia. The histopathological examination showed sclerainflammatory pathology and mediastinal pleural biopsy showed no definite pathology.

We were consulted when patient complained of acute onset breathlessness in the ward. CT pulmonary angiogram showed filling defects in the subsegmental branches of right and left pulmonary arteries suggestive of acute pulmonary embolism. The proximal extent of the mass was seen up to posterior carinal and subcarinal level [Figure 1]. There was no pulmonary parenchymal abnormality, no adenopathy or pleural effusion. Subsequently, bronchoscopic guided endobronchial ultrasound transbronchial needle aspiration (EBUS-TBNA) was planned.
Figure 1: Computed tomography pulmonary angiogram image at level of main carina, showing vertebral body destruction and soft-tissue lesion at D4-D5 level

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Bronchoscopy was done using the linear EBUS scope (BF-UC 180F; Olympus Medical Systems, Japan) with a compatible endoscopic ultrasound unit (EU-M E1; Olympus Medical Systems, Japan). The patient received nebulized lignocaine (4% solution) immediately before the procedure. Conscious sedation with injection midazolam and fentanyl were used - 2 mg/25 mcg respectively titrated up to 6 mg/150 mcg to achieve a good level of sedation. Topical 10% lignocaine spray was applied in the oropharynx. The procedure was done in the supine position through the oral route. The paraspinal mass was visualized with the EBUS scope placed in the medial wall of right and left main bronchi, seen best with the scope placed in the medial wall of left main bronchus [[Figure 2]. TBNA specimens were obtained using a dedicated, disposable, 22-gauge, EBUS needle (NA-201SX-4022 Olympus Medical Systems, Japan), using the jabbing method under real-time ultrasound control. Continuous suction was applied with a dedicated 20 ml syringe (VacLok) while the catheter was moved back and forth for up to a maximum of 10 times. Four passes were made from each side of the carina with the scope placed along the medial wall of right and left main bronchi.
Figure 2: Endobronchial ultrasound image of subcarinal area shows the mass with transbronchial needle aspiration needle in it. The mass appears as homogeneous well-defined round structure, in the upper part of image, with specs of calcification (whitish dots) in it

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Bedside cytology showed epitheliod cell granulomas suggestive of TB [Figure 3]. AFB stain was negative in the TBNA smear. Cytology of the aspirate showed no malignant cells. Polymerase chain reaction (PCR) of the TBNA aspirate (multiplex PCR, Mycobacterium) was positive for M. tuberculosis species. Gram stain and culture of the aspirate ruled out pyogenic or fungal infection. Patient was started on isoniazid, rifampicin, ethambutol and pyrazinamide according to World Health Organization (WHO) recommended weight regimen. He was discharged with anti-tubercular medications and vitamin K antagonists for pulmonary embolism. After 1 month of follow-up, he had significant relief of back pain and repeat erythrocyte sedimentation rate was 30 mm/h when compared to earlier value of 105 mm/h, 1 month back. TBNA aspirate culture by Mycobacterium growth indicator tube (MGIT, colorimetric based method) was negative for M. tuberculosis species. At 3 months follow-up, patient had remarkable clinical improvement with complete subsidence of back pain.
Figure 3: Photomicrograph of transbronchial needle aspiration aspirate showing Epitheliod cell Granulomas (H and E, ×400)

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   Discussion Top


The first modern case of spinal TB was described in 1779 by Percival Pott. [4] There are two distinct types of spinal TB, the classic form or spondylodiscitis and an increasingly common atypical form which is spondylitis without disc involvement. [5] The anterior aspect of the verte­bral body adjacent to the subchondral plate is commonly involved. [6]

Differential diagnosis of spinal TB includes pyogenic and fungal infections as well as metaststic and primary spinal tumors and it may be difficult when only clinical and radiographic findings are considered. [7] CT provides bony detail while MRI evaluates the involvement of soft-tissue and abscess formation. In comparison to pyogenic discitis, the most distinguishing feature of spinal TB is bony destruction with relative preservation of the intervertebral disc and heterogeneous enhancement. In pyogenic discitis, bone destruction and homogenous enhancement is more frequently observed. [8] The presence of an abscess and bone fragments differentiate spinal TB from neoplasia and if there is any doubt an image-guided biopsy is indicated. [9] In 88.5-96.4% of the cases, a CT guided FNAC biopsy is helpful and yields a diagnosis. [10],[11]

Spinal TB is a medical disease and anti-TB drugs have a main role in the recovery and response of patients. [12] Combination of rifampicin, isoniazid, ethambutol and pyrazinamide for 2 months followed by combination of rifampicin and isoniazid for a total period of 6, 9, 12 or 18 months is the most frequent protocol used for treatment of spinal TB. [13] The proposed regimen of WHO with total duration of 6 months consists of primary treatment with isoniazid, rifampicin, pyrazinamide and ethambutol for 2 months followed by 4 months of therapy with isoniazid and rifampicin. American Thoracic Society recommends 9 months of treatment with the same 4 drugs for initial 2 months followed by 7 months of therapy with isoniazid and rifampicin in the continuation phase, whereas the Canadian Thoracic Society recommends a total time of treatment as long as 9-12 months.

CT guided biopsy was attempted twice in this patient, but futile. Possible reasons could be: (1) The bulk of the lesion was pre-vertebral and located anteriorly in the spinal column. (2) The biopsy and FNAC were taken from the posterior spinal column along with the bone biopsy, which was taken from posterior spinal pedicle, and the bulk of lesion was located anteriorly in the spinal column. (3) As the patient was partially treated with anti-TB medication there might have been peripheral healing and aspirates taken from the periphery of the lesion repeatedly showed only degenerated cellular pathology.

Our patient presented with Pott's spine, however no definitive diagnosis could be made with the best available tests, hence we tried aspiration through endobronchial route via bronchoscopy (EBUS). To the best of our knowledge, this is the first reported case from India of EBUS TBNA from Pott's spine in a patient with acute pulmonary embolism.


   Conclusion Top


Base on the above report it can be concluded that endobronchial ultrasound guide needle aspiration is a safe procedure for difficult to diagnose pre/para-vertebral soft-tissue lesions, provided the lesion involves D4 vertebral level (at the level of main carina). It can be tried as second choice if CT guided biopsy is negative and there is diagnostic dilemma.

 
   References Top

1.Rezai AR, Lee M, Cooper PR, Errico TJ, Koslow M. Modern management of spinal tuberculosis. Neurosurgery 1995;36:87-97.  Back to cited text no. 1
    
2.Turgut M. Spinal tuberculosis (Pott′s disease): Its clinical presentation, surgical management, and outcome. A survey study on 694 patients. Neurosurg Rev 2001;24:8-13.  Back to cited text no. 2
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3.Barnes PF, Bloch AB, Davidson PT, Snider DE Jr. Tuberculosis in patients with human immunodeficiency virus infection. N Engl J Med 1991;324:1644-50.  Back to cited text no. 3
    
4.Sai Kiran NA, Vaishya S, Kale SS, Sharma BS, Mahapatra AK. Surgical results in patients with tuberculosis of the spine and severe lower-extremity motor deficits: A retrospective study of 48 patients. J Neurosurg Spine 2007;6:320-6.  Back to cited text no. 4
    
5.Pertuiset E, Beaudreuil J, Lioté F, Horusitzky A, Kemiche F, Richette P, et al. Spinal tuberculosis in adults. A study of 103 cases in a developed country, 1980-1994. Medicine (Baltimore) 1999;78:309-20.  Back to cited text no. 5
    
6.Hidalgo JA, Alangaden G, Cunha BA.Pott Disease: Tuberculous Spondylitis. New York: WebMD LLC; 2008. Available from: http://www.emedicine.medscape.com/article/226141-overview. [Last cited on 2010 Oct 15].  Back to cited text no. 6
    
7.Nussbaum ES, Rockswold GL, Bergman TA, Erickson DL, Seljeskog EL. Spinal tuberculosis: A diagnostic and management challenge. J Neurosurg 1995;83:243-7.  Back to cited text no. 7
    
8.Chang MC, Wu HT, Lee CH, Liu CL, Chen TH. Tuberculous spondylitis and pyogenic spondylitis: Comparative magnetic resonance imaging features. Spine (Phila Pa 1976) 2006;31:782-8.  Back to cited text no. 8
    
9.Gupta RK, Agarwal P, Rastogi H, Kumar S, Phadke RV, Krishnani N. Problems in distinguishing spinal tuberculosis from neoplasia on MRI. Neuroradiology 1996;38 Suppl 1:S97-104.  Back to cited text no. 9
    
10.Kang M, Gupta S, Khandelwal N, Shankar S, Gulati M, Suri S. CT-guided fine-needle aspiration biopsy of spinal lesions. Acta Radiol 1999;40:474-8.  Back to cited text no. 10
    
11.Mondal A, Misra DK. CT-guided needle aspiration cytology (FNAC) of 112 vertebral lesions. Indian J Pathol Microbiol 1994;37:255-61.  Back to cited text no. 11
    
12.Bakhsh A. Medical management of spinal tuberculosis: An experience from Pakistan. Spine (Phila Pa 1976) 2010;35:E787-91.  Back to cited text no. 12
    
13.Jain AK. Tuberculosis of the spine: A fresh look at an old disease. J Bone Joint Surg Br 2010;92:905-13.  Back to cited text no. 13
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    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

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