منابع مشابه
Rare presentation of osteoarticular tuberculosis.
The varied clinical presentation of osteoarticular tuberculosis makes the diagnosis an enigma. This report underlines the fact that osteoarticular tuberculosis can present in the most atypical pattern. It also emphasises the need for a high index of clinical suspicion and the low threshold for tissue biopsy for establishing the diagnosis.
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INTRODUCTION Tuberculosis of calcaneum is a rare entity. Osteoarticular tuberculosis of foot is uncommon and that of calcaneum is very rare. In children, diagnosis is often delayed as clinical presentation is non-specific and awareness is low due to its rare presentation. Also pediatric tuberculosis has traditionally received a lower priority than adult TB in National TB programmes. CASE PRES...
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Congenital tuberculosis is a rare disease with a high mortality rate. Congenital tuberculosis is considered the result of mother-to-child transmission from the placenta to the fetus, through the ingestion of the amniotic fluid, or via transplacental transmission through the umbilical vein. Given the non-specific clinical signs of tuberculosis, it is usually difficult to diagnose it. The case of...
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Tuberculosis is an infectious disease, commonly affecting the lungs. However, tuberculosis primarily affecting the conjuctiva is rare. Symptoms and signs of unilateral conjunctivitis may masquerade as primary conjunctival tuberculosis. In an endemic country like India, laterality, chronicity and non-resolution of symptoms with steroids are indications for pursuing a biopsy earlier than later. W...
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Tuberculosis is one of the oldest scorches of mankind that has not left this world even today. The disease is more common in the developing countries. Oral tuberculosis has been considered in 0.1-5% of all tuberculous infections. Mostly, the oral tuberculous lesions are secondary to pulmonary tuberculosis, but rarely primary lesions may occur. Primary lesions occur due to direct inoculation of ...
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ژورنال
عنوان ژورنال: Indian Heart Journal
سال: 2018
ISSN: 0019-4832
DOI: 10.1016/j.ihj.2018.10.340