scholarly journals Fever of unknown origin as the major manifestation of subacute thyroiditis

Author(s):  
Ahmad Housin ◽  
Marc P Pusztaszeri ◽  
Michael Tamilia

Summary Fever of unknown origin is a commonly encountered medical problem. Most common causes include infections, malignancy, and connective tissue diseases. Endocrine causes are rare but are well documented. While fever is common in some endocrine disorders, fever of unknown origin as the sole presenting feature is very rare. We describe a case report of a 63-year-old male who presents with fever of unknown origin. Imaging and biopsy results confirmed the diagnosis of subacute thyroiditis. He was started on prednisone with a good response. We conclude that subacute thyroiditis should be considered in the work up of fever of unknown origin even in the absence of classical signs and symptoms. Learning points Fever of unknown origin is a rare sole presentation of subacute thyroiditis. The classic signs and symptoms may not be manifest at the time of presentation. Normal thyroid function tests and elevated markers of inflammation often make infections, malignancy and autoinflammatory conditions the prime consideration. Imaging of the thyroid gland may point to a morphologic aberration and prompt a thyroid biopsy. After exclusion of infection, a rapid response to steroids may be both diagnostic and therapeutic.

2011 ◽  
Vol 4 ◽  
pp. CMAMD.S6763 ◽  
Author(s):  
Mohamad S. Abdelbaky ◽  
Howaida E. Mansour ◽  
Shafika I. Ibrahim ◽  
Iman A. Hassan

Objective To estimate the prevalence of connective tissue diseases in patients presenting with fever of unknown origin (FUO). Patients and Methods In this study thirty patients diagnosed as FUO (Group 1), in 2008, were included in an observational study and diagnostic workup. Additionally, retrospective analysis of seventy patients’ files (Group 2), for patients who presented with prolonged unexplained pyrexia to the same hospital in the previous two years, was performed. Patients were subjected to: full clinical assessment including full history taking, thorough clinical examination, laboratory investigations including the basic investigations for patients with prolonged fever, complete blood count, erythrocytes sedimentation rate, urine analysis and culture, blood culture, sputum culture and plain chest X ray. Further diagnostic work up and/or procedures were requested according to the potential diagnostic clues (PDC) present in every patient. Results Out of 100 FUO patients, 50% were found to have infectious diseases, 24% were found to have connective tissue diseases, 8% miscellaneous causes and 7% neoplastic diseases ( P < 0.05). In 11 patients no definite cause for FUO could be identified. Connective tissue patients were: eight systemic lupus patients (33.3%), five patients with familial mediterranean fever (20.8%), four patients with rheumatoid arthritis (16.6%), three patients (12.5%) with Still's disease and Rheumatic fever and one patient with Behçet syndrome/Crohn's disease (4.3%), ( P < 0.05). Conclusions Despite the advanced technology, FUO remains a challenging medical problem. Infections were the most common cause of FUO in Egypt, confirming the trends found in other parts of the world. There was an increased prevalence of connective tissue patients presented with prolonged unexplained fever. A keen clinical eye, meticulous history taking and repeated physical examination remained the most important diagnostic tools in FUO patients.


2020 ◽  
Author(s):  
Abir Bou Khalil ◽  
Walid Alam ◽  
Abdul Rahman Bizri

Abstract Background: Subacute thyroiditis (SAT) is a rare but well-established cause of fever of unknown origin (FUO) and should be considered in the differential of patients presenting with fever of unknown origin. Few reports in the English literature where published about Subacute thyroiditis manifesting as fever of unknown origin. Subacute thyroiditis may be hard to detect by physicians based on history and physical exam if the systemic manifestations are absent. Methods: An observational retrospective review of 375 charts of patients presenting with thyroiditis to the American University of Beirut Medical Center between January 1995 and June 2015. Inclusion criteria included patients who have subacute thyroiditis based on the American Thyroid Association and American Association of Clinical Endocrinologists guidelines and fever of unknown origin based on Durak and Street’s definition. All patients that do not fit both inclusion criteria were excluded. The patients’ demographics, clinical presentation, laboratory and diagnostic findings, and treatments used were analyzed. Results: 375 charts were reviewed. 31 patients had SAT of which 13 patients had fever of unknown origin before diagnosing subacute thyroiditis. 13 charts were not available for screening. Symptoms of hyperthyroidism including palpitations, neck tenderness and weight loss were not present in all patients. Elevated markers of inflammation mainly ESR and CRP were raised when screened for.Conclusions: The diagnosis of subacute thyroiditis should be considered in patients presenting with fever of unknown origin and elevated inflammatory markers, even in the absence of suggestive clinical symptoms.


2018 ◽  
Vol 2018 ◽  
pp. 1-8
Author(s):  
Rishi Raj ◽  
Srujana Yada ◽  
Aasems Jacob ◽  
Dileep Unnikrishnan ◽  
Wael Ghali

An 80-year-old Caucasian male presented with fever of 3-week duration. Outpatient workup for infectious etiologies was negative and due to persistent fever, he was hospitalized for further evaluation of fever of unknown origin (FUO). Physical examination and laboratory studies remained unremarkable; however a follow-up CT scan of chest, abdomen, and pelvis with contrast done to rule out malignancy as an underlying cause of FUO revealed heterogeneous thyroid gland with surrounding hazy changes suggestive of thyroiditis. Thyroid function tests confirmed the diagnosis of subacute thyroiditis. The patient was started on prednisone with good response in his symptoms and was eventually discharged to home. The importance of our case lies in the fact that diagnosing subacute thyroiditis in the absence of classical symptoms of neck pain can be challenging and a physician should have a very high index of suspicion especially in an elderly patient where FUO can be the sole presentation.


2021 ◽  
Vol 8 (11) ◽  
pp. 1842
Author(s):  
Naveen Gandla ◽  
Sheela A. Bharani ◽  
Tushar P. Shah

Background: In an era of advance science of modern technologies, many diseases are diagnosed and excluded rapidly and now Fever of Unknown Origin (FUO) has been redefined for any fever of 380C lasting for more than 7 days without any clear cause. The aetiology varies according to different geographical regions, socioeconomical status, age, prevalence of resistance to antimicrobial drugs and genetic susceptibility.Methods: It was a descriptive cross sectional, hospital-based study, carried out on 150 children from August 2018 to May 2020. All cases in the age group of 2 months to 18 years with fever of >38.0°C, lasting for more than 7 days without a clear source were included.Results: The mean age of presentation was 5.8 years±Standard Deviation of 3.7 years with male to female ratio was 1.4:1. Nearly half of the cases, presented with the duration of fever between 8-14 days. Enteric fever in 52%, tuberculosis in 13.3% and acute lymphoblastic leukemia (ALL) in 8.5% were three common etiologies found in this study. Amongst all cases of FUO, infective causes were seen in 113 (75.3%) followed by malignancies in 15(10%) cases. In 10 (6.7%) cases, cause could not be established.Conclusions: Enteric fever and tuberculosis were the leading etiologies from infective subgroup of FUO. ALL was the commonest cause from malignancies sub group. FUO presenting with low haemoglobin, platelet is a pointer towards malignancy. Occurrence of FUO with infectious diseases and malignancies was found in younger age group as compared to connective tissue diseases. 


Cureus ◽  
2021 ◽  
Author(s):  
Bhagyalakshmi Satyanarayan ◽  
Anupama Sahu ◽  
Satish K Prasad ◽  
Sarita Kumari

2017 ◽  
Vol 17 (1) ◽  
pp. 86-87 ◽  
Author(s):  
Fatima Amar Bahowairath ◽  
Nicholas Woodhouse ◽  
Samir Hussain ◽  
Mujahid Al Busaidi

2021 ◽  
Vol 80 (Suppl 1) ◽  
pp. 966.2-966
Author(s):  
B. Egeli ◽  
S. Ugurlu

Background:Adult-Onset Still’s disease (AOSD) is an autoinflammatory condition characterized by fever, rash, and arthritis. The diagnosis of AOSD is made by excluding common causes of fever of unknown origin which are infections, malignancies, autoimmune conditions and medication adverse effects. As it is a diagnostic challenge, further data on highlighting clinical and laboratory findings are necessary on guiding clinicians.Objectives:Our main objective is to present our single tertiary center experience of patients diagnosed with AOSD.Methods:This retrospective study was conducted at a tertiary rheumatology center. Patients were diagnosed with AOSD using Yamaguchi’s criteria and followed between 2007 and 2020. Demographic, clinical and laboratory information was retrieved from the patient chars. Treatment-related and prognostic information were also noted with additional information from phone call interviews.Results:The study includes 69 patients (23 M, 46 F). The mean age of diagnosis was 33.86±14.3. The presenting signs and symptoms of the patients are shown in Figure 1. The laboratory findings supporting the diagnosis at initial encounter are summarized in Table 1. The mean corticosteroid dose at initial diagnosis was 29.7±18 mg. In addition to corticosteroid treatment these patients were followed with different glucocorticoid-sparing agents. Methotrexate was the choice of treatment in 54 patients with the mean dose of 14.5±3.43 mg. Eight patients were treated with leflunomide, seven with anti-TNF agents, seven with tocilizumab, nineteen with anakinra and four with canakinumab.Figure 1.The presenting signs and symptoms of the patientsConclusion:In conclusion, the most common presenting symptoms in our AOSD cohort were fever and salmon-colored rash. In the differential diagnosis of fever of unknown origin especially with rash, AOSD should be considered. Corticosteroid was the main treatment modality. In patients who are unresponsive to conventional immunosuppressive treatment, biologic agents can be an alternative.Table 1.The laboratory findings at initial encounterMean ± Standard DeviationFerritin (ng/mL)3179.46±6503.56ESR (mm/h)77.43±28.47CRP (mg/L)102.29±70.39Leukocyte Count (cells/L)13147.3±4640.9ESR (mm/h)80±28.48CRP (mg/L)105.15±54.67Leukocyte Count (cells/L)12427.14±6530.43Disclosure of Interests:None declared


2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 694.1-694
Author(s):  
R. Talarico ◽  
C. Stagnaro ◽  
F. Ferro ◽  
A. Figliomeni ◽  
L. Carli ◽  
...  

Background:Giant cell arteritis (GCA) represents the most common primary vasculitis of the elderly, that usually involves large and medium sized arteries. The wide spectrum of clinical manifestations can extensively vary, from cranial symptoms, such as headache, jaw claudication or visual alterations, to constitutional symptoms, like fever, weight loss or asthenia. Fever of unknown origin (FUO) may sometimes represents the initial symptom of GCA and when it is not associated with other typical GCA features, the diagnosis can be unluckily delayed.Objectives:The primary aim of the study was to identify the prevalence of GCA patients presenting as FUO. The secondary aims were to identify the delays in the diagnosis and to compare them between the last two decades.Methods:Epidemiological and clinical data of 274 GCA patients followed in the last 20 years in our Unit were analysed. We quantified the latency period between the onset of signs and symptoms and the final diagnosis of GCA in terms of months.Results:One hundred and eighty-five patients (49 males and 136 females, mean ± SD age at the onset 71±7 years) had shown at the onset signs and symptoms suggestive of GCA (new onset headache and/or scalp pain 86%, jaw claudication 39%, vision loss 35%, abnormal temporal artery on examination 49%, dizziness 31%) while 89 patients (33 males and 56 females, mean age at the onset 69±4 years) were sent to our attention just for the onset of FUO and for an increase of erythrocyte sedimentation rate and C-reactive protein not otherwise justified. After an extensive work-up aimed at excluding any kind of infection, malignancy or hematological disorder, the patients with FUO performed a temporal artery biopsy (TAB) and/or a (18)F-fluorodeoxyglucose positron emission tomography (18F-FDG PET). The results from histology and/or imaging allowed us to perform the diagnosis of GCA in all cases; moreover the main PET alterations reported were characterized by a (18)FDG uptake of the aortic arch and its major braches, including the carotid, subclavian, thoracic aorta and, less frequently, the abdominal aorta. Considering the different decades, the mean latency period between the onset of FUO and the diagnosis of GCA was 6±3 months in the decade from 2000 to 2010 and 3±2 months in the last decade, that was significantly higher compared with the mean latency period between the onset of signs and symptoms suggestive of GCA and the definitive diagnosis (3±1 months) in the other patients of the cohort in the first decade. Notably the latency period between the onset of signs and symptoms suggestive of GCA and the definitive diagnosis was more close (2±1 months) to the latency period of diagnosis in FUO presenting GCA in the last decade.Conclusion:Our data underline that there is a major focus on the diagnosis of GCA, even when the presentation is not typical; this is probably due to the major knowledge reached in the last decade, to an improved sensibilization regarding the different profiles of presentation and surely on the bigger use of 18F-FDG PET in the work-up of GCA patients.Acknowledgments:noneDisclosure of Interests:None declared


2013 ◽  
Vol 84 (5) ◽  
pp. 733 ◽  
Author(s):  
Jong Ho Kim ◽  
Kwi Hyun Bae ◽  
Yeon Kyung Choi ◽  
In Gyoon Ha ◽  
Keun Gyu Park ◽  
...  

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