scholarly journals Polymerase chain reaction compared to other laboratory findings and to clinical evaluation in the diagnosis of cutaneous tuberculosis and atypical mycobacteria skin infection

2009 ◽  
Vol 48 (1) ◽  
pp. 27-35 ◽  
Author(s):  
Cristina Martinez Zugaib Abdalla ◽  
Zilda Najjar Prado de Oliveira ◽  
Mirian N. Sotto ◽  
Kátia Ramos Moreira Leite ◽  
Flávio Canellas Canavez ◽  
...  
2019 ◽  
Vol 7 ◽  
pp. 2050313X1986945
Author(s):  
Abdülkadir Sari ◽  
Yaşar Mahsut Dinçel ◽  
Ibrahim Halil Erdogdu ◽  
Hakan Sezgin Sayıner ◽  
Ismail Agir ◽  
...  

Background: Tuberculosis osteomyelitis is rarely seen in the diaphyseal bones. It may be confused with Brodie’s abscess due to similar clinical, radiological and laboratory findings. Late diagnosis of the disease causes bone destruction. Tuberculosis osteomyelitis of the bone is a rare condition caused by the Mycobacterium tuberculosis. Its incidence has increased in Western countries in recent years due to HIV infection, increasing elderly population and emerging resistant strains. The slow progress of tuberculous osteomyelitis, due to lack of significant elevations in the laboratory values and changes in the radiographic appearance, often leads to confusion with the subtypes of subacute osteomyelitis, defined as Brodie’s abscess. These two low-virulence clinical cases often lead to delays in diagnosis and progressive bone destruction. Case presentation: We report a 65-year-old male patient who presented to our clinic with pain, swelling and sensitivity in the left leg. Diagnosed with infection in the tibia, the patient had undergone antibiotherapy. However, the patient’s symptoms were not resolved and we performed bone curettage and cementation. M. tuberculosis-specific DNA was detected by real-time polymerase chain reaction and the M. tuberculosis complex was produced from the perioperative samples. Conclusion: In conclusion, histopathological examination and polymerase chain reaction are essential before surgery of subacute and chronic osteomyelitis with atypical clinical, laboratory and radiological findings for early diagnosis and accurate treatment.


2013 ◽  
Vol 30 (5) ◽  
pp. 1485-1490 ◽  
Author(s):  
Maruthai Kathirvel ◽  
Vallayyachari Kommoju ◽  
Usharani Brammacharry ◽  
Thirumurugan Ravibalan ◽  
Nandikolla Ravishankar ◽  
...  

2019 ◽  
Vol 53 (2) ◽  
Author(s):  
Leah Antoinette M. Caro-Chang ◽  
Eileen Liesl A. Cubillan

A 33-year-old male had a 22-year history of generalized xanthogranulomas but had a normal lipid profile. He also developed ulcerating plaques on his arm and back that were consistent with cutaneous tuberculosis on histopathologic and polymerase chain reaction PCR studies. In a normolipemic patient with generalized xanthogranulomas, a reactive granulomatous response of histiocytes to infection is explored since these share a common CD 14+ precursor with the macrophages that are vital in tuberculosis.


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