scholarly journals Orbital tuberculosis: perspectives from Victoria, Australia

2018 ◽  
Vol 256 (12) ◽  
pp. 2443-2448 ◽  
Author(s):  
Anthony Yao ◽  
Craig Aboltins ◽  
Alan A. McNab ◽  
Cesar Salinas-La Rosa ◽  
Justin Denholm ◽  
...  
Keyword(s):  
2014 ◽  
Vol 44 (3) ◽  
pp. 148-151 ◽  
Author(s):  
Saurbhi Khurana ◽  
Neelam Pushker ◽  
Sreedhara Shankara Naik ◽  
Seema Kashyap ◽  
Seema Sen ◽  
...  

2015 ◽  
Vol 4 (1) ◽  
pp. 99
Author(s):  
AbdelrahmanE.M Ezzat
Keyword(s):  

Orbit ◽  
1993 ◽  
Vol 12 (1) ◽  
pp. 27-30
Author(s):  
Rosemarie Desouza ◽  
Chris Desouza ◽  
Mark D'souza ◽  
I. M. Vora
Keyword(s):  

2004 ◽  
Vol 46 (5) ◽  
pp. 291-294 ◽  
Author(s):  
Bráulio F.T. Oliveira ◽  
Fernanda C. Takay ◽  
Tatiana M. Shida ◽  
Ruth M. Santo ◽  
Abelardo C. Souza Jr. ◽  
...  

PURPOSE: To describe three cases of orbital tuberculosis, with their clinical characteristics and respective diagnostic procedures, showing the importance of histopathology for the correct diagnosis. PATIENTS AND METHODS: Three patients diagnosed and treated for orbital tuberculosis, in the "Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo" during the years of 1999 and 2001. RESULTS: All of the patients were female and referred a chronic evolution of swelling of one eyelid associated or not with other symptoms. They had not HIV infection. Two of them had positive epidemiology for tuberculosis. However, the search for systemic evidence of the disease and staining for bacilli (Ziehl-Neelsen method) were negative in all three patients. In all the cases, only the biopsy with immunohistochemical analysis could confirm the diagnosis. COMMENTS: Orbital involvement is a rare ocular manifestation of tuberculosis. Even in a tertiary hospital, few cases, if any, are diagnosed per year. However, the global incidence and prevalence of M. tuberculosis infections is not under control yet, and it has been a serious public health problem. Thus, one must be aware of the possibility of tuberculosis among the orbital diseases.


1970 ◽  
Vol 3 (2) ◽  
pp. 210-213 ◽  
Author(s):  
C Chakraborti ◽  
R Biswas ◽  
M Mondal ◽  
U Muknopadhya ◽  
J Datta

Background: Orbital tuberculosis is rare even in endemic areas. The disease may involve soft tissue, lacrimal gland, or the periosteum or bones of the orbital wall. Case: We present an Indian girl, who presented with a slowly growing left-sided superotemporal orbital mass, with no significant previous medical history. The swelling turned to an abscess and burst spontaneously giving rise to a discharging sinus. The discharge was negative for any organism on Gram and Giemsa staining. A tuberculin skin test was strongly positive. Incisional biopsy showed caseating granuloma and Langhan’s giant cells suggestive of tubercular aetiology. The patient responded well to tuberculous chemotherapy. Conclusion: Although tuberculous dacryoadenitis is a very rare manifestation of tuberculosis, still the possibility should be entertained in a slowly growing mass of the lacrimal gland, especially in developing countries where the prevalence of tuberculosis is high. Key words: Tuberculosis, lacrimal gland, histopathology DOI: http://dx.doi.org/10.3126/nepjoph.v3i2.5281 Nepal J Ophthalmol 2011; 3(2): 210-213


1995 ◽  
Vol 11 (1) ◽  
pp. 27-31 ◽  
Author(s):  
Sasikala Pillai ◽  
Timothy J. Malone ◽  
Juan Carlos Abad
Keyword(s):  

2006 ◽  
Vol 73 (4) ◽  
pp. 361-363 ◽  
Author(s):  
Suvasini Sharma ◽  
Monica Juneja ◽  
Ravindra Kumar Saran ◽  
Atul Mohan Kochhar
Keyword(s):  

Orbit ◽  
2017 ◽  
Vol 36 (5) ◽  
pp. 264-272 ◽  
Author(s):  
Ruchi Mittal ◽  
Savitri Sharma ◽  
Suryasnata Rath ◽  
Manas Ranjan Barik ◽  
Devjyoti Tripathy

2017 ◽  
Vol 3 ◽  
pp. 2513826X1775111
Author(s):  
Kalila Steen ◽  
Jeffrey Fialkov

We describe an interesting case of a 57-year-old man who presented with a rare case of orbital tuberculosis masquerading as sarcoidosis. The varied presentation of orbital tuberculosis may only become evident once a tissue diagnosis is available. Therefore, the dilemma in diagnosis of this rare condition highlights the need for definitive diagnosis through tissue biopsy by a plastic surgeon.


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