Create issue ticket

1,467 Possible Causes for ascitic fluid lymphocytosis

Did you mean: ascitic fluid, lymphocytosis

  • Angioedema

    Clin Imaging. 2017 May - Jun;43:122-126. doi: 10.1016/j.clinimag.2017.03.001. Epub 2017 Mar 8. Author information 1 Department of Radiology, Northwestern Memorial Hospital, Northwestern University Feinberg School of Medicine, 676 N. Saint Clair St., Suite 800, Chicago, IL 60611, United States. 2 Department of Radiology, Emory[…][]

  • Spontaneous Bacterial Peritonitis

    Low-protein-concentration ascitic fluid predisposes to spontaneous bacterial peritonitis.[] RESULTS: In 105 cases of ascitic fluid analyses, 27 (25.72%) had positive ascitic fluid culture whereas 78 (74.28%) had negative ascitic fluid culture.[] Guidelines suggest that patients with ascitic fluid protein below 15 g/l receive fluoroquinolones to prevent SBP.[]

  • Hereditary Angioedema

    Hereditary and acquired angioedema are of outstanding clinical importance, as edematous attacks associated with these conditions can thrust afflicted patients into mortal danger. Currently, C1 inhibitor concentrate – a human blood product – is available as a replacement therapy. In view of the limited number of[…][]

  • Hereditary Angioedema Type 1

    Hereditary angioedema type 1 is an autosomal dominant disease characterized by C1 esterase inhibitor deficiency and the onset of edema, abdominal pain and erythema marginatum. Clinical features of HAE are largely indistinguishable across all types, but type 1 is characterized by a prodromal period in which a[…][]

  • Persistent Polyclonal B-cell Lymphocytosis

    Abstract Persistent polyclonal B-cell lymphocytosis (PPBL) is a rare clinical condition, characterized by a persistent, generally moderate lymphocytosis, generally due to[] Abstract We present a case of persistent polyclonal B-cell lymphocytosis (PPBL).[] Abstract We document a case of persistent lymphocytosis in which the characteristic binucleated circulating lymphocytes were shown immunologically to be polyclonal B-cells[]

  • Hepatitis C

    Symptomatic acute hepatitis C occurs in only about 15% of patients who are infected with hepatitis C virus (HCV). Acute hepatitis C is most often diagnosed in the setting of post-exposure surveillance, or seroconversion in high-risk individuals (eg, health-care professionals or injecting drug users) previously known[…][]

  • Hereditary Angioedema Type 2

    Hereditary angioedema is an autosomal dominant and life-threatening disorder characterized by recurrent episodes of non-pitting edema affecting the skin, respiratory system and digestive tracts and caused by a congenital deficiency or function defect of the C1 esterase inhibitor. Preseptal cellulitis is defined as[…][]

  • Hereditary Angioedema Type 3

    Hereditary angioedema (HAE) type 3 stems from mutations in Hageman factor XII, unlike types 1 and 2, in which either deficiency or impaired function of C1 esterase inhibitor (C1-INH) is the principal cause of angioedema, profound abdominal pain, and erythema marginatum. The recurrent, unpredictable, and abrupt onset[…][]

  • Ascites

    Ascitic fluid can become infected ( spontaneous bacterial peritonitis ), often with pain and fever.[] However, ascitic fluid cytology was negative for malignant cells. A differential diagnosis of tubercular mass was made.[] The ascitic fluid analysis showed 921 cells/mm 3 with mononuclear predominance (93.6%), elevated total proteins and a slightly elevated serum-ascites albumin gradient.[]

  • Malignant Ascites

    Only three patients had positive ascitic fluid cultures.[] We report a case in which EGFR exon 20 T790M mutation was detected by repeat ascitic fluid examination.[] In ascites fluid, a significant accumulation of CD8( ) cytotoxic T-cells and Tregs was observed compared to peripheral blood.[]

Further symptoms

Similar symptoms