Adult-onset Still’s disease with secondary macrophage activation syndrome: a case report

نویسندگان

چکیده

We describe a case of adult-onset Still’s disease (AOSD) with secondary macrophage activation syndrome. AOSD is rare unknown origin. Rarely it’s complicated by syndrome, which life-threatening disorder. Because the diagnosis essential for exclusion and complications are life-threatening, it mandatory prompt extensive diagnostic workup treatment.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A Case of Adult Onset Stills Disease

Adult-onset Still's disease (AOSD) is characterized by fever, rash, and joint pain and may lead to chronic arthritis. The cause of AOSD is unknown, and it is rare. We encountered a patient with adult-onset Still's disease following a sore throat and fever. The patient was a 40-year-old woman who consulted our hospital because of a sore throat, fever and arthritis. She was admitted and treated w...

متن کامل

Macrophage Activation Syndrome as the First Impression of Kawasaki Disease; A Case Report

Introduction Macrophage activation syndrome (MAS) is a rare and life-threatening complication of Kawasaki Disease (KD) that is usually diagnosed at the same time or after KD. We report a case of MAS as the initial manifestation of KD. Case Report A previously healthy 3-year old girl was admitted to the pediatric infectious di...

متن کامل

[Macrophage activation syndrome associated with adult-onset Still's disease].

Macrophage activation syndrome (MAS) is a rare and potentially lethal disease, resulting from uncontrolled activation and proliferation of T lymphocytes and macrophages. Adult-onset Still's disease (AOSD) is an inflammatory disease. AOSD resemble reactive MAS in its symptoms and laboratory data. Moreover, AOSD per se induces MAS. It is, therefore, quite difficult to differentiate these syndrome...

متن کامل

Hyperreactio Luteinalis with early-onset HELLP syndrome: A case report

Introduction: Hyperreactio Luteinalis (HL) is a rare benign condition in pregnancy which is characterized by bilaterally multicystic ovarian enlargement containing theca lutein cysts caused by increased production of hCG. HL is mostly associated with hydatidiform mole and multiple pregnancies. Correspondence: Azin Alavi, ...

متن کامل

Crohn’s Disease with Oral Onset - A Case Report

Background: Crohn’s disease is an inflammatory bowel disease that can affect any part of the gastrointestinal (GI) tract including the mouth. Bowel symptoms are predominant. Oral involvement may precede the GI symptoms. This case report presents a patient affected by Crohn’s disease with oral onset. Case presentation: We present a 30-year-old pregnant woman complaining of chronic, ...

متن کامل

ذخیره 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: Italian Journal of Medicine

سال: 2023

ISSN: ['1877-9352', '1877-9344']

DOI: https://doi.org/10.4081/itjm.2023.1595