Inflammation of a serous membrane.
A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease.
Hereditary inflammation conditions, characterized by recurrent episodes of systemic inflammation. Common symptoms include recurrent fever, rash, arthritis, fatigue, and secondary AMYLOIDOSIS. Hereditary autoinflammatory diseases are associated with mutations in genes involved in regulation of normal inflammatory process and are not caused by AUTOANTIBODIES, or antigen specific T-LYMPHOCYTES.
A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow.

Extra-articular rheumatoid arthritis: prevalence and mortality. (1/33)

OBJECTIVE: The prevalence and distribution of extra-articular manifestations of rheumatoid arthritis (ExRA) and associated mortality were studied retrospectively in a cohort of RA patients admitted to University Hospital, Malmo, Sweden, during the period 1990-94. RESULTS: Of 489 patients who fulfilled the 1987 ACR criteria for RA, 37 manifested onset of ExRA, predominantly serositis and cutaneous vasculitis, during the period, corresponding to a cumulative incidence of 7.9%. The occurrence of ExRA was independent of disease stage. Among patients with ExRA, 1 death/4.3 person-years at risk (pyr) occurred, as compared with 1 death/11.4 pyr in the non-ExRA subgroup. The age- and sex-adjusted mortality rate ratio was 2.49 (95% confidence interval 1.43-4.03). The major cause of death among ExRA cases was heart disease, which occurred in 9/13 cases (69%) in comparison to the expected 2.4 cases. CONCLUSION: In this series, serositis and cutaneous vasculitis were predominant extra-articular manifestations of RA; and mortality was greater in the ExRA than in the non-ExRA subgroup, perhaps due to a high frequency of associated heart disease.  (+info)

Serosal complications of single-agent low-dose methotrexate used in gestational trophoblastic diseases: first reported case of methotrexate-induced peritonitis. (2/33)

Methotrexate (MTX) is a folate antagonist widely used both as an anticancer drug and as an immunosupressant. Administration of an 8-day methotrexate and folinic acid regime may be associated with pleuritic chest pain and pneumonitis. We have reviewed the toxicity seen in 168 consecutive patients treated with low-dose MTX for persistent trophoblastic disease. Twenty-five per cent of patients developed serosal symptoms, pleurisy was the commonest complaint. The majority of patients had mild to moderate symptoms which were controlled with simple analgesia and did not necessitate a change in treatment; 11.9% had severe symptoms which necessitated a change in treatment. One patient developed a pericardial effusion and a second patient developed severe reversible peritoneal irritation. The possible aetiology and pathophysiology of methotrexate-induced serosal toxicity is discussed.  (+info)

Serial antinuclear antibodies titre in pleural and pericardial fluid. (3/33)

The antinuclear antibodies (ANA) test has been a cornerstone of the evaluation of connective tissue disease. The aim of this study was to investigate the diagnostic value of the ANA test in pleural or pericardial effusions of unknown causes. Over a 3-yr period, a total of 126 pleural fluid and 30 pericardial fluid samples were analysed. ANA tests were performed using a commercially available kit. The ANA kit used an indirect immunofluorescent antibody method with a human epithelial (HEP-2) cell line as substrate. Patients with high fluid ANA titre (>1:160) received a second aspiration 2 weeks after the initial aspiration if diagnosis was not confirmed. ANA results were positive in 39 pleural and 10 pericardial fluid samples. All but one of the effusions with positive ANA testing were exudative. Eleven pleural or pericardial effusions due to active systematic lupus erythematosus were identified and all had high ANA titres (1:160) with various staining patterns. Thirty-eight of 145 patients (26%) with effusions of nonlupus aetiologies had positive ANA testing in pleural or pericardial fluid. Thirteen of these 38 patients had high ANA titre. Malignant or paramalignant effusions constituted 11 of the 13 samples. In conclusion, although a negative antinuclear antibodies test makes a diagnosis of lupus serositis unlikely, high antinuclear antibodies titres in pleural or pericardial fluid are not diagnostic of lupus serositis even when as high as 1:5,120. An unexplained high antinuclear antibodies titre in pleural or pericardial effusion warrants search for malignancy.  (+info)

Polyserositis in pigs due to generalized Escherichia coli infection. (4/33)

A fibrinous polyserositis syndrome due to generalized Escherichia coli infection in pigs was observed in 13 out of 17 systematically monitored herds. The mortality rate was approximately 0.1% among liveborn pigs. The occurrence was usually sporadic but a minor enzootic was observed in one herd. Most of the affected pigs succumbed during first or second week of life but cases were observed throughout the suckling period. The clinical signs included marked depression, anorexia, rough haircoat, laboured respiration and death in two to five days. Predominant gross pathological lesions were signs of septicaemia and a voluminous, gelatinous and fibrinous exudate in the pleural, the pericardial and the peritoneal cavities. Frequently also a firbinous polyarthritis and a fibrinous pneumonia were present. The majority of the isolated invasive E. coli strains were nonhaemolytic. Serologically 11 different E. coli O groups were encountered. O group most frequently represented was 020. None of the examined E. coli strains belonged to the serogroups which frequently are associated with enteropathogenicity in pigs.  (+info)

Mycoplasma alligatoris sp. nov., from American alligators. (5/33)

Mycoplasmas were isolated from multiple tissues of diseased American alligators (Alligator mississippiensis). This paper presents biochemical, serological and molecular genetic characterizations of a lethal pathogen of alligators for which the name Mycoplasma alligatoris sp. nov. is proposed. The type strain is A21JP2T (ATCC 700619T).  (+info)

Mortality patterns in Malaysian systemic lupus erythematosus patients. (6/33)

A retrospective analysis of the case records of 494 systemic lupus erythematosus (SLE) patients under follow-up at University Hospital, Kuala Lumpur during 1976-1990 was performed. Overall mortality was 20.2% (100 patients). The causes of death were infection (30%), renal (15%), respiratory (14%), neurological (5%), cardiovascular (7%), other causes (2%) and unknown (27%). Active SLE was a contributing factor in 19% of the deaths. The patients who died had significantly more renal disease, neurological disease, serositis or thrombocytopenia by the end of the first year of disease compared to the survivors. As in other series, infection and active SLE remain important causes of death.  (+info)

A case of erythema nodosum and serositis associated with myelodysplastic syndrome. (7/33)

Myelodysplastic syndrome (MDS) is a heterogenous group of stem cell disorders usually characterized by progressive refractory cytopenias, which could progress to acute myeloid leukemia. MDS may be associated with a wide spectrum of skin lesions, including neoplastic cell infiltration, Sweet's syndrome, pyoderma gangrenosum, erythema elevatum diutinum, vasculitis, and panniculitis. However, erythema nodosum is rarely associated with MDS. Unusual rheumatologic manifestations in patients with MDS also have been reported, which range from asymptomatic serological abnormalities to classic connective tissue disorders such as Sjogren's syndrome, relapsing polychondritis, systemic lupus erythematosus, rheumatoid arthritis and mixed connective tissue disease. However, concurrent erythema nodosum and serositis has rarely been reported. We describe a case of MDS with erythema nodosum and immune-mediated pericardial effusion in a 34-year-old woman.  (+info)

Serosal appendicitis: incidence, causes and clinical significance. (8/33)

BACKGROUND: Serosal appendicitis is a histopathological diagnosis of an inflammatory reaction on the surface of the appendix caused by an extra appendiceal source of inflammation. OBJECTIVE AND METHODS: A retrospective review of a pathology database in a district general hospital identified patients with serosal appendicitis and a preoperative diagnosis of appendicitis. Two groups emerged: patients with serosal appendicitis secondary to a known cause of intra-abdominal inflammation and those in whom the cause remained unknown. The groups were compared with respect to postoperative complications, referral to outpatient clinics, admissions and procedures by case-note analysis. RESULTS: The incidence of serosal appendicitis was 0.01% (19/1379); 17 women; mean age 31.63 (10.49) years. Lanz incision was used in 16 patients, midline laparotomy in two and laparoscopy in one. A preoperative ultrasound scan was carried out in 5 of 19 patients. The cause of serosal appendicitis was confirmed in eight patients (intraoperatively or postoperatively) and remained unknown in 11 patients. The groups were comparable with respect to age, sex and mean follow-up. No significant difference was observed between them with respect to the above parameters. CONCLUSIONS: No further investigation is necessary in patients who undergo an appendicectomy but in whom the pathological diagnosis is serosal appendicitis. However, considering the patient demographics and the fact that patients with serosal appendicitis have probably undergone an unnecessary appendicectomy, the proportion of patients who underwent ultrasound scanning and diagnostic laparoscopy was small.  (+info)

Serositis is a medical term that refers to inflammation of the serous membranes, which are thin layers of tissue that line the inner surfaces of body cavities and surround organs such as the heart, lungs, and abdomen. The serous membranes produce a lubricating fluid called serous fluid that helps reduce friction between internal organs and enables them to move smoothly against each other.

Inflammation of these membranes can result in excessive production of serous fluid, leading to the accumulation of fluid in the surrounding body cavities. This accumulation can cause symptoms such as chest pain, coughing, difficulty breathing, or abdominal swelling and discomfort.

Serositis is often associated with various medical conditions, including autoimmune diseases like rheumatoid arthritis, lupus, and Sjogren's syndrome. Infections, cancers, and certain medications may also cause serositis. Treatment typically involves addressing the underlying condition causing the inflammation and managing symptoms with medications such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, or immunosuppressive agents.

Familial Mediterranean Fever (FMF) is a hereditary inflammatory disorder that primarily affects people of Mediterranean ancestry, including populations from Turkey, Armenia, Arab countries, and Jewish communities from the Middle East. It is caused by mutations in the MEFV gene, which provides instructions for making a protein called pyrin or marenostrin.

The main features of FMF include recurrent episodes of fever, serositis (inflammation of the membranes lining the abdominal cavity, chest cavity, or heart), and polyserositis (inflammation affecting multiple serous membranes simultaneously). The attacks usually last between 12 and 72 hours and can be associated with severe abdominal pain, joint pain, and skin rashes.

The diagnosis of FMF is based on clinical criteria, family history, and genetic testing. Treatment typically involves the use of colchicine, an anti-inflammatory medication that helps prevent attacks and reduces the risk of long-term complications such as amyloidosis, a condition characterized by the buildup of abnormal protein deposits in various organs.

Early diagnosis and treatment of FMF are essential to prevent complications and improve quality of life for affected individuals.

Hereditary autoinflammatory diseases (HAIDs) are a group of rare, inherited disorders characterized by recurrent episodes of inflammation in the body. These diseases are caused by mutations in genes that regulate the innate immune system, which is the body's first line of defense against infection.

In HAIDs, the immune system mistakenly attacks the body's own cells and tissues, leading to symptoms such as fever, rash, joint pain and swelling, abdominal pain, and inflammation of internal organs. The symptoms can vary in severity and frequency, and may be triggered by factors such as stress, infection, or physical exertion.

Examples of HAIDs include Familial Mediterranean Fever (FMF), Tumor Necrosis Factor Receptor-Associated Periodic Syndrome (TRAPS), Cryopyrin-Associated Periodic Syndromes (CAPS), and Blau syndrome/Early Onset Sarcoidosis.

The diagnosis of HAIDs is often challenging due to the rarity of these conditions and overlapping symptoms with other diseases. Genetic testing, medical history, physical examination, and laboratory tests are used to confirm the diagnosis and determine the specific type of HAID. Treatment typically involves medications that suppress the overactive immune system, such as biologic agents that target specific components of the immune system.

Systemic Lupus Erythematosus (SLE) is a complex autoimmune disease that can affect almost any organ or system in the body. In SLE, the immune system produces an exaggerated response, leading to the production of autoantibodies that attack the body's own cells and tissues, causing inflammation and damage. The symptoms and severity of SLE can vary widely from person to person, but common features include fatigue, joint pain, skin rashes (particularly a "butterfly" rash across the nose and cheeks), fever, hair loss, and sensitivity to sunlight.

Systemic lupus erythematosus can also affect the kidneys, heart, lungs, brain, blood vessels, and other organs, leading to a wide range of symptoms such as kidney dysfunction, chest pain, shortness of breath, seizures, and anemia. The exact cause of SLE is not fully understood, but it is believed to involve a combination of genetic, environmental, and hormonal factors. Treatment typically involves medications to suppress the immune system and manage symptoms, and may require long-term management by a team of healthcare professionals.

... is seen in numerous conditions: Lupus erythematosus (SLE), for which it is one of the criteria, Rheumatoid arthritis ... Serositis refers to inflammation of the serous tissues of the body, the tissues lining the lungs (pleura), heart (pericardium ... Causes of Serositis. diagnosispro.com. URL: http://en.diagnosispro.com/differential_diagnosis-for/serositis/11271-154.html ...
serositis Archived 2016-03-03 at the Wayback Machine at eMedicine Dictionary "Sugar-coated spleen". Drugs.com. (Webarchive ... serositis) covering the organ. The spleen is commonly affected and often referred to as sugar-coated spleen. The liver and ... Hyaline Serositis Hyaloserositis. Online Medical Dictionary. URL: http://cancerweb.ncl.ac.uk/cgi-bin/omd?hyaloserositis. ...
Systemic JIA may have internal organ involvement such as hepatosplenomegaly, lymphadenopathy, serositis, hepatitis, or ...
Serositis with pleural and pericardial effusions are seen in up to 10% of these patients. On the other hand, flares of lupus ...
Males tend to have more seizures, kidney disease, serositis (inflammation of tissues lining the lungs and heart), skin problems ... Serositis: Pleurisy (inflammation of the membrane around the lungs) or pericarditis (inflammation of the membrane around the ...
... unless serositis or synovitis is present. Elevations of CRP in the absence of clinically significant inflammation can occur in ...
... serositis, lasting less than 72 hours. It is caused by mutations in the MEFV gene, which codes for the protein pyrin.[citation ...
... otitis and sclerosing serositis. This syndrome has not been observed with other such beta blockers. This drug has been ...
... serositis, and oral ulcers. The cause of diffuse proliferative glomerulonephritis (DPGN) depends on the severity of the disease ...
... serositis and anaemia. JIA is a chronic disorder, which if neglected, can lead to serious complications. However, with regular ...
Fever Anemia Thrombocytopenia Renal Neuro changes SOAP BRAIN MD Serositis Oral ulcers Arthritis Photosensitivity, pulmonary ...
... serositis MeSH C23.550.470.756 - suppuration MeSH C23.550.470.756.100 - abscess MeSH C23.550.470.756.200 - cellulitis MeSH ...
Serositis Nephrotic syndrome Hereditary angioedema Other rare causes[citation needed] Meigs syndrome Vasculitis Hypothyroidism ...
Fatigue Serositis-inflammation of the tissues lining the heart and lungs. Anti-histone antibodies in 95% of cases among those ...
Cases of drug-induced hepatitis can manifest with systemic signs of an allergic reaction including rash, fever, serositis ( ...
Serositis is seen in numerous conditions: Lupus erythematosus (SLE), for which it is one of the criteria, Rheumatoid arthritis ... Serositis refers to inflammation of the serous tissues of the body, the tissues lining the lungs (pleura), heart (pericardium ... Causes of Serositis. diagnosispro.com. URL: http://en.diagnosispro.com/differential_diagnosis-for/serositis/11271-154.html ...
serositis answers are found in the Tabers Medical Dictionary powered by Unbound Medicine. Available for iPhone, iPad, Android ... "Serositis." Tabers Medical Dictionary, 24th ed., F.A. Davis Company, 2021. Nursing Central, nursing.unboundmedicine.com/ ... nursingcentral/view/Tabers-Dictionary/733250/all/serositis. Serositis. In: Venes DD, ed. Tabers Medical Dictionary. F.A. Davis ... Serositis [Internet]. In: Venes DD, editors. Tabers Medical Dictionary. F.A. Davis Company; 2021. [cited 2023 September 22]. ...
The population of patients receiving dialysis in the United States is largely due to universal government funding for treatment of end-stage renal disease (ESRD) and the high prevalence of predisposing conditions such as diabetes and hypertension. Patients with ESRD are encountered on a regular basis in US emergency departments.
Serositis. No. No. Macrophage activation syndrome. No. Yes. Disease remission, ever. No. No. ...
Acute promyelocytic leukemia (APL) is a distinct variant of acute myeloid leukemia (AML). It is classified as AML M3 by the old French-American-British (FAB) system and as APL with translocation between chromosomes 15 and 17-that is, t(15;17)-by the World Health Organization (WHO) classification system.
Inside our analysis, the frequency of serositis in persistently anti-dsDNA negative patients resulted greater than 80%. Inside ... serositis resulted even more regular in the anti-dsDNA considerably ? (79 individuals, 82.3%) set alongside the anti-dsDNA + ... our analysis, the frequency of serositis in persistently anti-dsDNA negative patients resulted greater than 80%. the cut-off ...
Cattaneo, A., Cattane, N., Galluzzi, S., Provasi, S., Lopizzo, N., Festari, C., Ferrari, C., Guerra, U. P., Paghera, B., Muscio, C., Bianchetti, A., Volta, G. D., Turla, M., Cotelli, M. S., Gennuso, M., Prelle, A., Zanetti, O., Lussignoli, G., Mirabile, D., Bellandi, D., & 8 othersGentile, S., Belotti, G., Villani, D., Harach, T., Bolmont, T., Padovani, A., Boccardi, M. & Frisoni, G. B., 31 Aug 2016, (E-pub ahead of print) In: Neurobiology of Aging.. Research output: Contribution to journal › Article › peer-review ...
Member has active systemic features (e.g., fever, evanescent rash, lymphadenopathy, hepatomegaly, splenomegaly, or serositis); ... Systemic features (e.g., fever, evanescent rash, lymphadenopathy, hepatomegaly, splenomegaly, or serositis); ... Systemic features (e.g., fever, evanescent rash, lymphadenopathy, hepatomegaly, splenomegaly, or serositis); ...
Serositis Medicine and Dentistry 25% * Bone Medicine and Dentistry 25% View full fingerprint ...
Dive into the research topics where T-Cell Signaling and Development is active. These topic labels come from the works of this organisations members. Together they form a unique fingerprint ...
Faber, B. G., Frysz, M., Hartley, A. E., Ebsim, R., Boer, C. G., Saunders, F. R., Gregory, J. S., Aspden, R. M., Harvey, N. C., Southam, L., Giles, W., Le Maitre, C. L., Wilkinson, J. M., van Meurs, J. B. J., Zeggini, E., Cootes, T., Lindner, C., Kemp, J. P., Davey Smith, G. & Tobias, J. H., 20 Jan 2023, (E-pub ahead of print) In: Arthritis and Rheumatology. 75, 6, p. 900-909 10 p.. Research output: Contribution to journal › Article (Academic Journal) › peer-review ...
I have been a lecturer within the School of Pharmacy since June 2010 and my research focuses upon proteases with particular emphasis on their role in immune signalling and disease.. Currently my work focuses upon the DUB/USP17 family of deubiquitinating enzymes where we have shown that USP17 (DUB-3) is induced in response to cytokines, chemokines and growth factors (IL-4, IL-6, IL-8, SCF1, EGF) and that it regulates cell growth and movement. Subsequently, we have demonstrated that USP17 modulates signalling through the Ras/MEK/ERK pathway due to its regulation of Ras processing and localisation. Moreover, we have identified a novel isoform of the protease Ras converting enzyme 1 (RCE1), which is involved in Ras processing, and shown that it is ubiquitinated and that its deubiquitination by USP17 can regulate its localisation and function. We have also shown that USP17 is over-expressed in a range of tumour tissues and we are currently assessing USP17 as a potential cancer therapeutic ...
Dive into the research topics of Expression of Toll-like receptor 2 is up-regulated in monocytes from patients with chronic obstructive pulmonary disease. Together they form a unique fingerprint. ...
TY - JOUR. T1 - The carcinogenic action of crystalline silica. T2 - a review of the evidence supporting secondary inflammation-driven genotoxicity as a principal mechanism. AU - Borm, Paul J A. AU - Tran, Lang. AU - Donaldson, Kenneth. PY - 2011. Y1 - 2011. N2 - In 1987 the International Agency for Research on Cancer (IARC) classified crystalline silica (CS) as a probable carcinogen and in 1997 reclassified it as a Group 1 carcinogen, i.e., that there was sufficient evidence for carcinogenicity in experimental animals and sufficient evidence for carcinogenicity in humans. The Working Group noted that "carcinogenicity in humans was not detected in all industrial circumstances studied, carcinogenicity may be dependent on inherent characteristics of the crystalline silica or on external factors affecting its biological activity or distribution of its polymorphs." This unusual statement that the physicochemical form of the CS influences its carcinogenicity is well understood at the toxicological ...
Serositis: Pleurisy (inflammation of the membrane around the lungs) or pericarditis (inflammation of the membrane around the ...
Acute promyelocytic leukemia (APL) is a distinct variant of acute myeloid leukemia (AML). It is classified as AML M3 by the old French-American-British (FAB) system and as APL with translocation between chromosomes 15 and 17-that is, t(15;17)-by the World Health Organization (WHO) classification system.
Visceral serositis in acute Epstein-Barr virus infectious mononucleosis. Lucia CATTANEO, Gregorio P. MILANI *, Sebastiano A. ...
C-reactive protein levels are not necessarily elevated; high levels raise the concern for infection and/or serositis. ... Manifestations may include abdominal pain resulting from serositis, nausea, vomiting, manifestations of bowel perforation, and ...
The clinical manifestations of drug-induced lupus erythematosus are generally milder with arthralgias and serositis being the ... SLE causes of AAP include serositis, vasculitis, ischemic gut, pseudo-obstruction, pancreatitis, acalculous cholecytitis, and ... and during flare-ups of the disease and is often found in conjunction with pleural effusions as part of a generalized serositis ...
Rash, serositis, hematologic and joint flares were associated with an increase in temperature. Renal flares decreased as the ... Humidity was significantly associated with joint and serositis flares. PM2.5 concentration was significantly associated with ... rash, joints, serositis and haematologic flares.. While the studys findings show a strong association between changes in ...
Nolde, J. M., Hillis, G. S., Atkins, E., Von Huben, A., Marschner, S., Chan, J., Reid, C. M., Nelson, M. R., Figtree, G., Chalmers, J., Usherwood, T., Rodgers, A., Chow, C. K. & Schlaich, M. P., 1 Nov 2022, In: Journal of Hypertension. 40, 11, p. 2271-2279 9 p.. Research output: Contribution to journal › Article › peer-review ...
Signs and symptoms of drug-induced lupus reported in BETASERON-treated patients have included rash, serositis, polyarthritis, ...
Hematological abnormalities (leukocytopenia, anemia, thrombocytopenia) and serositis were not associated with an SSc pattern. ...
... and serositis (pleural and/or pericardial). One was a case of biopsy-proven cutaneous lupus erythematosus. No significant ...
Thom, O. N. N., Keijzers, G., McD Taylor, D., Fatovich, D. M., Finucci, D. P. P., Furyk, J., Jin, S-W. W., Macdonald, S. P. J., Mitenko, H. M. A. M. A., Richardson, J. R. R., Ting, J. Y. S. Y. S., Gibbs, C. R. R. & Chalkley, D. R. R., 1 Oct 2016, In: Emergency Medicine Australasia. 28, 5, p. 603-606 4 p.. Research output: Contribution to journal › Article › peer-review ...
Dive into the research topics where Igor Chernyavsky is active. These topic labels come from the works of this person. Together they form a unique fingerprint ...
... serositis, myalgia and arthritis.. Note=A IL6 promoter polymorphism is associated with a lifetime risk of development of Kaposi ...
The supporting examinations showed abnormal blood cell counts, positive antinuclear antibody profile, serositis, and neuropathy ...
  • Rash, serositis, hematologic and joint flares were associated with an increase in temperature. (hospitalhealthcare.com)
  • PM2.5 concentration was significantly associated with rash, joints, serositis and haematologic flares. (hospitalhealthcare.com)
  • Type 1 lupus: Encompasses the signs and symptoms that are classically attributed to inflammation , including arthritis , rash, serositis, nephritis , central nervous system lupus , and certain laboratory findings. (lupus.org)
  • Systemic-onset juvenile idiopathic arthritis (sJIA) is a type of auto-inflammatory disease that shows clinical manifestations such as fever, rash, hepatosplenomegaly, serositis, and synovitis ( 1 1. (scielo.br)
  • Serositis refers to inflammation of the serous tissues of the body, the tissues lining the lungs (pleura), heart (pericardium), and the inner lining of the abdomen (peritoneum) and organs within. (wikipedia.org)
  • Patients with FMF type 1 have short episodes of inflammation and serositis including fever, peritonitis, synovitis, pleuritis, and rarely, pericarditis and meningitis. (lu.se)
  • Patients display attacks associating recurrent fever, arthritis, serositis and skin manifestations [1]. (efim.org)
  • The time predating disease was shorter and the number of autoantibodies was greater in those individuals with serositis as a presenting symptom in comparison to those with arthritis and skin manifestations as the presenting symptoms. (nih.gov)
  • Furthermore, 1 in 5 healthy individuals and serositis and recurrent peritonitis, arthritis, pleuritis in Armenia are heterozygous carriers of one of the several or erysipelas-like skin disease. (who.int)
  • Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent fever and serositis. (turkiyeklinikleri.com)
  • The clinical manifestations of drug-induced lupus erythematosus are generally milder with arthralgias and serositis being the predominant symptoms, and major organ involvement is usually absent. (lww.com)
  • The supporting examinations showed abnormal blood cell counts, positive antinuclear antibody profile, serositis, and neuropathy. (journaltocs.ac.uk)
  • Inulin is added in feed, the absorption of minerals can be promoted, while intestinal beneficial bacterium being made to increase, inhibits the growth of harmful bacteria, and it is each Kind bulk pharmaceutical chemicals interaction, can effectively improve duckling immunity, to preventing kind duck infectious serositis, bird flu and Escherichia coli Disease etc. has good effect, can effectively reduce duckling morbidity and mortality, improves duckling survival rate. (google.com)
  • There was evidence of acute serositis. (ijpmonline.org)
  • The girl did not appear toxic, and no evidence of organomegaly or serositis was present. (consultant360.com)
  • URL: http://en.diagnosispro.com/differential_diagnosis-for/serositis/11271-154.html Archived 2012-06-29 at archive.today. (wikipedia.org)
  • Same Day Diagnosis of Extrapulmonary TB (TB Serositis and TB Meningitis). (who.int)
  • FMF is characterized by relatively short, usually 1- to 3-day, episodes of fever accompanied with serositis, synovitis or skin rash. (genome.gov)
  • Apart from fever, the most common feature of FMF is serositis, which manifests as abdominal pain due to peritonitis in up to 90% of patients. (logicalimages.com)
  • The relationship between certain forms of intestinal obstruction, chronic peritonitis and multiple serositis. (nih.gov)