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Correct Answer - A Ans: A. Lead poisoning Findings Microcytic Anemia - Iron Deficiency Hypersegmented Neutrophils - B12 and Folic Acid Deficiency Young & No H/o Of Alcohol Consumption [Patient came with a history of Fatigue and Tiredness] - Chronic Alcoholism can be ruled out Hemolytic Anemia - may demonstrate red blood cell fragments called schistocytes, red blood cells that look like spheres (spherocytes), and/or red blood cells missing small pieces (bite cells). An increased number of newly made red blood cells (reticulocytes) may also be a sign of bone marrow compensation for anemia.
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A 23-year-old male presented with history f fatigue& tiredness On investigation, he found t hv Hb values of 9gm%, MCV of 101 FL. peripheral smear examination showed microcytic RBC and hypersegmented neutrophils. Which is most probable etiologyAnonymous voting
  • A.Lead poisoning
  • B.Iron deficiency anemia
  • C. Chronic alcoholism
  • D.Hemolytic anemia
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Correct Answer - D Ans: D. Unidirectional locomotion of neutrophils Chemotaxis is defined as a unidirectional movement of leukocytes up to a concentration gradient of chemotactic molecules. All granulocytes, monocytes and to a lesser extent lymphocytes respond to chemotactic stimuli with varying rates of speed. Chemoattractants are exogenous or endogenous. Exogenous agents are bacterial products. Endogenous mediators are: Components of complement pathway C5a Products of lipoxygenase pathway LTB4 Cytokines particularly those of chemokine families.
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What is the main feature of chemotaxis as observed in white blood cells?Anonymous voting
  • A.Increased random movement of neutrophils
  • B.Increased adhesiveness to intima
  • C.Increased phagocytosis
  • D.Unidirectional locomotion of neutrophils
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Correct Answer - A Answer- A- Immunochromatography assays HBV chronic carriers are those in whom HBsAg persists for more than 6 months in the presence of HBeAg or anti-HBe. HBsAg may persist for years after the loss of HBeAg. The most useful detection methods are enzyme-linked Immunosorbent assay for HBV antigens and antibodies and PCR for viral DNA -Jawetz 27/e pg- 504 Serological assays detect the host immune response (antibodies to HCV) or a viral antigen (HBsAg, HCVcAg). They are based on the immunoassay principle and are available in the form of rapid diagnostic tests (RDTs) or laboratory-based enzyme immunoassays (EIAs), chemiluminescence immunoassays (CLIAs) and electrochemiluminescence immunoassays (ECLs).
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HbsAg is based on which principleAnonymous voting
  • A.Immunochromatography assays
  • B.Chemiluminescene
  • C.ELISA
  • D.Immunofluroscence
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Correct Answer - D Ans. is 'd' i.e., None The morphologic consequences of embolic occlusion of the pulmonary arteries depend on the size of the embolic mass and the general state of the circulation. Large emboli may impact in the main pulmonary artery or its major branches or lodge at the bifurcation as a saddle embolus. Sudden death often ensues, owing largely to the blockage of blood flow through the lungs. Death may also be caused by acute failure of the right side of the heart (acute cor pulmonale). Smaller emboli can travel out into the more peripheral vessels, where they may cause infarction. In patients with adequate cardiovascular function, the bronchial arterial supply can often sustain the lung parenchyma despite obstruction to the pulmonary arterial system. Under these circumstances, hemorrhages may occur, but there is no infarction of the underlying lung parenchyma. Only about 10% of emboli actually cause infarction. Although the underlying pulmonary architecture may be obscured by the suffusion of blood, hemorrhages are distinguished by the preservation of the pulmonary alveolar architecture; in such cases, resorption of the blood permits reconstitution of the preexisting architecture.
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Pulmonary infarction occurs with all except -Anonymous voting
  • A.Saddle embolus at bifurcation
  • B.Blockage of 2nd and 3rd gen end arteries
  • C.Arterioles are blocked
  • D.None
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Correct Answer - B Ans. is 'b' i.e., Dermatomyositis Dermatomyositis is a connective-tissue disease related to polymyositis that is characterized by inflammation of the muscles and the skin. It is a systemic disorder that may also affect the joints, the esophagus, the lungs, and, less commonly, the heart. On the muscle biopsy, there are two classic microscopic findings of dermatomyositis. They are : mixed B- & T-cell perivascular inflammatory infiltrate and perifascicular muscle fiber atrophy. It is associated with autoantibodies, especially anti-Jol antibody
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Perifascicular atropy of muscle fibres is seen in?Anonymous voting
  • A.Steroid myopathy
  • B.Dermatomyositis
  • C.Inclusion body myositis
  • D.Nemaline myopathy
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Some patients with severe form of Idiopathic infantile hypercalcemia, presnt with phenotypic features similar to which of the following?Anonymous voting
  • A.Williams syndrome
  • B.Potters syndrome
  • C.Angelman syndrome
  • D.VHL syndrome
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Correct Answer - D Ans. is 'd' i.e., Seen in teratoma o Psammoma bodies represent a process of dystrophic calcification. o Single necrotic cells may constitute seed crystals that become encrusted by the mineral deposits. The progressive acquisition of outer layers may create lamellated configurations, called psammoma bodies because of their resemblance to grains of sand. o Psammoma bodies are seen in : papillary cancer of thyroid, meningioma, papillary serous cystadenocarcinoma of ovary.
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True about Psammoma bodies are all except ?Anonymous voting
  • A.Seen in meningioma
  • B.Concentric whorled appearance
  • C.Contains Calcium deposits
  • D.Seen in teratoma
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True about Psammoma bodies are all except ?Anonymous voting
  • A.Seen in meningioma
  • B.Concentric whorled appearance
  • C.Contains Calcium deposits
  • D.Seen in teratoma
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NEET PG25 Recall available in group @doctorusmle
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Ans. is 'b' i.e., Spongiform change in brain o The classic histologic appearance in Creutzfeldt-Jakob disease is spongiform change in the gray matter : in all six cortical layers in the cerebral cortex or with diffuse involvement of the cerebellar molecular layer. These vacuoles appear glassy or eosinophilic and may coalesce. Neuronal loss and gliosis are also seen.
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What is the histological appearance of brain in Creutzfeldt-Jakob disease -Anonymous voting
  • A.Neuronophagia
  • B.Spongiform change in brain
  • C.Microabscesses
  • D.Demyelination
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Repost from TgId: 1168687131
Vitiligo is associated with the following exceptAnonymous voting
  • A.Addison's disease
  • B.Men syndrome
  • C.Pernicious anemia
  • D.Crohns disease
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