FAMILIAL RECURRING POLYSEROSITIS: A DISEASE ENTITY
1959; American College of Physicians; Volume: 51; Issue: 6 Linguagem: Inglês
10.7326/0003-4819-51-6-1253
ISSN1539-3704
AutoresRobert J. Priest, Robert K. Nixon,
Tópico(s)Sympathectomy and Hyperhidrosis Treatments
ResumoArticle1 December 1959FAMILIAL RECURRING POLYSEROSITIS: A DISEASE ENTITYROBERT J. PRIEST, ROBERT K. NIXONROBERT J. PRIESTSearch for more papers by this author, ROBERT K. NIXONSearch for more papers by this authorAuthor, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-51-6-1253 SectionsAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail ExcerptI. INTRODUCTIONFamilial recurring polyserositis is a unique disease entity almost entirely limited to persons of Armenian, Syrian or Jewish ethnic origin. Janeway and Mosenthal1in 1908 described a syndrome of recurrent abdominal pain in a Jewish school girl aged 16 years. All of her life she had suffered from recurring episodes of fever, leukocytosis and abdominal pain with abdominal rigidity and tenderness lasting one to two days and recurring at intervals of from one to four weeks. Siegal2, 3subsequently referred to this disease as "benign paroxysmal peritonitis," and Reimann,4in his discussion of periodic diseases, included it as...Bibliography1. JanewayMosenthal TCHO: An unusual paroxysmal syndrome, probably allied to recurrent vomiting, with a study of the nitrogen metabolism, Tr. A. Am. Physicians 23: 504, 1908. Google Scholar2. Siegal S: Benign paroxysmal peritonitis, Ann. Int. Med. 23: 1, 1945. LinkGoogle Scholar3. Siegal S: Benign paroxysmal peritonitis—second series, Gastroenterology 12: 234, 1949. CrossrefMedlineGoogle Scholar4. Reimann HA: Periodic disease: periodic fever, periodic abdominalgia, cyclic neutropenia, intermittent arthralgia, angioneurotic edema, anaphylactoid purpura and periodic paralysis, J. A. M. A. 141: 175, 1949. CrossrefMedlineGoogle Scholar5. ReimannMoadiéSemerdjianSahyoun HAJSPF: Periodic peritonitis: heredity and pathology, report of seventy-two cases, J. A. M. A. 154: 1254, 1954. CrossrefMedlineGoogle Scholar6. HellerSoharSherf HEL: Familial Mediterranean fever, Arch. Int. Med. 102: 50, 1958. CrossrefGoogle Scholar7. CattanMamou RH: 14 cas de maladie périodique dont 8 compliqués de néphropathies, Bull. et mém. Soc. méd. d. hôp. de Paris 67: 1104, 1951. MedlineGoogle Scholar8. MamouCattan HR: La maladie périodique (sur 14 cas personnels dont 8 compliqués de néphropathies), Semaine d. hôp. Paris 28: 1062, 1952. MedlineGoogle Scholar9. CamatteRouquetteRuiz GMM: Un cas de maladie périodique, Bull. et mém. Soc. méd. d. hôp. de Paris 69: 60, 1953. MedlineGoogle Scholar10. SiguierZaraFunck-BrentanoLagrue FMJLG: Réflexions sur la maladie dite périodique, Semaine d. hôp. Paris 29: 3649, 1953. Google Scholar11. BenhamouAlbouGriguer EAP: Les formes familiales de la maladie périodique, Algérie méd. 58: 1, 1954. MedlineGoogle Scholar12. SiguierSebaoun FJ: Maladie périodique avec crises de sialhorrhée et neutropénie cycliques, Bull. et mém. Soc. méd. d. hôp. de Paris 70: 27, 1954. MedlineGoogle Scholar13. SiguierZaraSebaoun FMJ: Formes aberrantes et frontiéres nosologiques de la maladie dite périodique, Bull. et mém. Soc. méd. d. hôp. de Paris 70: 31, 1954. MedlineGoogle Scholar14. Cattan R: Maladie périodique: dix observations et deux hypotheses, Bull. et mém. Soc. méd. d. hôp. de Paris 70: 43, 1954. MedlineGoogle Scholar15. Mamou H: Nouveaux cas de maladie périodique. Remarques biologiques et pathogéniques, Bull. et mém. Soc. méd. d. hôp. de Paris 70: 520, 1954. MedlineGoogle Scholar16. Mamou H: Maladie périodique amylogène, Semaine d. hôp. Paris 31: 388, 1955. MedlineGoogle Scholar17. Mamou H: La maladie périodique, 1956, Expansion Scientifique Française, Paris. Google Scholar18. Calligaris G: Due casi familiari de "malattia periodica," Minerva pediat. 5: 781, 1953. MedlineGoogle Scholar19. SturtzBurke GSEC: "Periodic peritonitis," J. Dis. Child. 92: 390, 1956. MedlineGoogle Scholar20. Nixon RK: Detection of splenomegaly by percussion, New England J. Med. 250: 166, 1954. CrossrefMedlineGoogle Scholar21. Reimann HA: Periodic disease: observations on old cases and report of new cases and of therapeutic trials, Arch. Int. Med. 92: 494, 1953. CrossrefGoogle Scholar22. BrickCajigas IBM: Benign paroxysmal peritonitis; surgical and histologic findings, New England J. Med. 244: 786, 1951. CrossrefMedlineGoogle Scholar23. BickelLasserre GR: La maladie de Siegal-Cattan-Mamou: péritonite paroxystique abactérienne avec réactions pleuropéricardiques et articulaires, forme clinique autonome et la maladie périodique de Reimann, Schweiz. med. Wchnschr. 87: 5, 1957. MedlineGoogle Scholar24. Kelly AR: Unpublished data. Google Scholar25. MamouMaret HR: Étude anatomo-clinique d'une épanalepsie méconnue chez un Arménien, Semaine d. hôp. Paris 32: 3197-3204 (Oct. 22) 1956. MedlineGoogle Scholar26. MamouGuérande HA: Néphrose lipoïdique et maladie périodique, Semaine d. hôp. Paris 29: 358, 1953. MedlineGoogle Scholar27. Tuqan NA: Periodic disease: a clinicopathologic study, Ann. Int. Med. 49: 885, 1958. LinkGoogle Scholar28. Shamma'a MH: Medical problems in Lebanon, New England J. Med. 257: 218, 1957. CrossrefMedlineGoogle Scholar29. Reimann HA: Periodic disease: probable syndrome including periodic fever, benign paroxysmal peritonitis, cyclic neutropenia, and intermittent arthralgia, J. A. M. A. 136: 239, 1948. CrossrefMedlineGoogle Scholar30. Reimann HA: Periodic disease, Medicine 30: 219, 1951. CrossrefMedlineGoogle Scholar31. Siegal S: Periodic disease, J. A. M. A. 141: 738, 1949. CrossrefGoogle Scholar32. Cooke RA: Gastrointestinal manifestations of allergy, Bull. New York Acad. Med. 9: 15, 1933. MedlineGoogle Scholar33. de VriesDanonNelkenHenig ADDE: Red cell abnormality and autoimmune antibody in periodic disease, Harefuah 52: 1, 1957. MedlineGoogle Scholar34. Willis WH: Treatment of benign paroxysmal peritonitis with para-aminobenzoic acid, J. A. M. A. 147: 654, 1951. CrossrefMedlineGoogle Scholar35. IsraelKeeterUrbachWillis HLELFEWD: Relief of chest pain by tetraethylammonium chloride, New England J. Med. 241: 738, 1949. CrossrefMedlineGoogle Scholar36. FosterWhipple DPGH: Fibrin values influenced by cell injury, inflammation, intoxication, liver injury, and the Eck fistula: notes concerning origin of fibrinogen in body, Am. J. Physiol. 58: 407, 1922. CrossrefGoogle Scholar This content is PDF only. To continue reading please click on the PDF icon. Author, Article, and Disclosure InformationAffiliations: Detroit, Michigan*Received for publication May 16, 1959.Presented at the Fortieth Annual Session of The American College of Physicians, Chicago, Illinois, April 21, 1959.From the Divisions of Gastroenterology and General Medicine, Henry Ford Hospital, Detroit, Michigan.Requests for reprints should be addressed to R. J. Priest, M.D., 2799 West Grand Boulevard, Detroit 2, Michigan. 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GEORGE, M.D., ROBERT E. WESTFALL, M.D.Familial paroxysmal polyserositisThe differential diagnosis of coronary artery disease and gastrointestinal disorders∗Polyserositis induced by psicofuranine in man and comparative toxicity in the rat, mouse, dog, chicken, and monkeyPeriodic Polyserositis (Periodic Disease)Recurrent polyserositis (familial mediterranean fever; Periodic disease)Electrocardiographic changes in recurrent polyserositis (“periodic disease”)Familial Mediterranean FeverPeriodic Fever with Renal AmyloidosisThe Genetic Approach to the Study of Gastrointestinal DiseaseFamilial Recurring Polyserositis Simulating Acute Surgical Condition of the AbdomenMedical genetics 1959Febbre Mediterranea Familiare (FMF) 1 December 1959Volume 51, Issue 6Page: 1253-1274KeywordsAbdominal painArthralgiaArthritisFeversHospital medicineLeukocytosisPathogenesisPeritonitisRisk managementThorax ePublished: 1 December 2008 Issue Published: 1 December 1959 PDF downloadLoading ...
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