​Pathology - Leukocytoclastic Vasculitis

​Pathology - Leukocytoclastic Vasculitis

Pathology - Leukocytoclastic Vasculitis  Leukocytoclastic vasculitis (hypersensitivity) Vasculitis refers to the inflammation of blood vessels. The precise source of this condition is not known, although it is believed to be triggered by the deposition o

​Pathology - Cryoglobulinemia

​Pathology - Cryoglobulinemia

Pathology - Cryoglobulinemia Possible causes encompass lymphoproliferative illnesses such as multiple myeloma, chronic lymphocytic leukemia (CLL), and non-Hodgkin lymphoma (NHL), as well as hepatitis C virus (HCV) infection. The causes of autoimmune syndr

​Pathology - Von Hippel-Lindau disease

​Pathology - Von Hippel-Lindau disease

Pathology - Von Hippel-Lindau disease This is an autosomal dominant condition that causes the deletion of the von Hippel-Lindau (VHL) gene, which is a tumor suppressor gene located on chromosome 3p. Study of diseases and their effects on the body. Heman

Pathology - Osler Weber Rendu Syndrome

Pathology - Osler Weber Rendu Syndrome

Pathology - Osler Weber Rendu Syndrome  Osler-Weber-Rendu Syndrome, also known as Hereditary Hemorrhagic Telangiectasia, is a medical condition. This is an autosomal dominant condition caused by mutations in TGF-Beta-binding proteins. It is more common

​Pathology - Kaposi Sarcoma

​Pathology - Kaposi Sarcoma

Pathology - Kaposi Sarcoma  Kaposi sarcoma is a type of cancer that affects the skin and other organs. The cause of this condition is still unknown, although researchers are investigating the possibility of a viral origin and its connection to the immune

​Pathology - Von Willebrand Disease

​Pathology - Von Willebrand Disease

Pathology - Von Willebrand Disease Von Willebrand disease is an autosomal dominant disorder characterized by a deficit in von Willebrand factor (vWF). Acquired von Willebrand disease is linked to cancer and autoimmune disorders, and is caused by reduced

Pathology - Hypercoagulable States

Pathology - Hypercoagulable States

Pathology - Hypercoagulable States The causes of inherited hypercoagulable conditions encompass Factor V Leiden (which involves resistance to activated protein C), prothrombin mutation, deficiency of protein C or S, deficiency of antithrombin III, and an

​Pathology -Disseminated Intravascular Coagulation (DIC)

​Pathology -Disseminated Intravascular Coagulation (DIC)

Pathology -Disseminated Intravascular Coagulation (DIC) These conditions, including abruptio placenta, amniotic fluid embolus, cancer, sepsis, trauma, acute pancreatitis, shock, and hemolytic transfusion reactions, are often associated with the occurrenc

​Pathology -Essential  and Secondary Hypertension

​Pathology -Essential  and Secondary Hypertension

Pathology -Essential and Secondary Hypertension Primary (idiopathic) hypertension (90%): Risk factors encompass advanced age, ethnicity, diabetes, tobacco use, excessive weight, and a positive familial background. Secondary (10%): Renal parenchymal dise