Background
Isolated involvement of bone marrow in sarcoidosis has not been reported commonly. Sarcoidosis is a systemic granulomatous disease of unknown origin, characterized by the presence of non-caseating granulomatous lesions. There should be high index of suspicion in patients having underlying lymphoproliferative malignancies.
Case presentation
We present a 27-year-old male, known case of chronic myeloid leukemia, presenting as fever of unknown origin diagnosed with isolated bone marrow sarcoidosis.
Splenic rupture is a potentially life-threatening condition associated with acute abdominal pain. Although rare, atraumatic spleen rupture (ASR) has been reported. It is not usually considered in the differential diagnosis of acute abdomen so often missed in emergency leading to high morbidity and mortality. We present the case of a 38-year-old male who presented with fever and acute abdominal pain, had atraumatic splenic rupture which was diagnosed early resulting in better outcome of patient.
Concomitant hepatitis A virus (HAV) and amoebic liver abscess are to be considered in patients with clinical signs and symptoms of fever, jaundice, and right upper quadrant pain, especially in endemic areas. Both diseases had similar epidemiology and identical mode of transmission, i.e., the feco-oral route. We report a case of a young female with simultaneous infection of HAV and amoebic liver abscess, emphasizing the role of dual infection and its clinical manifestations.
Tuberculosis (TB) and lung cancer are the leading causes of mortality and morbidity in the world. The burden of TB is significantly high in developing countries causing serious public health concern, and the incidence of lung cancer is also increasing all around the world with high mortality. Pulmonary TB coexisting with lung cancer can mask the underlying disorder producing diagnostic dilemma resulting in a delay in diagnosis leading to decreased survival of the patients. Here, we report a rare case of a 66-year-old male diagnosed with microbiologically confirmed TB along with coexisting small cell neuroendocrine carcinoma of the lung presenting with syndrome of inappropriate antidiuretic hormone.
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