A case report on leptospirosis with pseudohepatorenal syndrome
نویسندگان
چکیده
The spirochete Leptospira interrogans causes leptospirosis, a zoonosis. There are numerous clinical symptoms of leptospirosis. Clinical manifestations might range from subclinical infection with mild fever to severe jaundice and renal failure. Here, case leptospirosis acute failure, thrombocytopenia, hyperbilirubinemia is presented. A 51-year-old man presented fever, body aches, muscle colored urine, for 2 days. On serology report, L. AB IGM-CARD was weekly positive. In the Renal function test, urea creatinine values were high as well liver test abnormal. patient given 1 g ceftriaxone intravenously 100 mg doxycycline orally. Hepatorenal treatment supportive outcome It may have been overlooked when diagnosis confirmed.
منابع مشابه
PHACES syndrome with cataract and Horner’s syndrome: a case report
PHACES syndrome (Posterior Fossa Malformations, Hemangioma, Arterial Anomalies, Cardiac Defects and Coarctation of the Aorta, Eye Abnormalities, and Sternal Abnormalities or Ventral Developmental Defects) is a rare neurocutaneous syndrome, which characteristic feature is large segmental hemangioma. Extracutaneous involvement is an important cause of morbidity in this syndrome.<br /...
متن کاملLeptospirosis presenting as haemolytic uraemic syndrome: a case report
BACKGROUND Leptospirosis is a rare infectious disease especially in Western Countries. Renal involvement is a recognised complication of leptospirosis but leptospirosis-associated haemolytic uraemic syndrome is extremely rare and to our knowledge has only been reported once, in 1985. CASE PRESENTATION A 29-year-old male was transferred to our Renal Unit with fevers, myalgia and diarrhoeal ill...
متن کاملSheehan Syndrome: A Case Report
'rwo cases of post-partum amenorrhea with other clinical signs of She1ehan syndrom was studied at the Loghmandoleh Medical Center, National University of Iran. Clinical diagnosis was confirmed by appropriate laboratory work -up in the f.irSlt case and the patient was placed on the conventional end orga.n hormon substitutional therapy (Thyroid -Gonad -Adrenal) and was discharged in good cond...
متن کاملPendred Syndrome: A Case Report
In this article Pendred's syndrome, which is the combination of - congenital goitre with deafmutism, is discussed. This type of goitre is due to a special enzymatic defect, involving a process of hormonogenesis, which is respon-· sible for the incorporation of iodide in the tyrosine molecule. A case of pendred's syndrome is presented in a 16-year-old girl. This girl has never been able to...
متن کاملApert Syndrome: A Case Report
Apert syndrome is a genetic defect which was first described by Eugene Apert in 1906. itchr('39')s incidence is approximately one in 50000 births. This syndrome is many abnormalities in your body and Central Nervous System. rehabilitation can increase children and their parentchr('39')s quality of life.We report a case of Apert syndrome and his occupational therapy program.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Indian Journal of Case Reports
سال: 2022
ISSN: ['2454-129X', '2454-1303']
DOI: https://doi.org/10.32677/ijcr.v8i7.3488