1.Non-Infectious Diseases Causing Fever of Unknown Origin.
Journal of the Korean Medical Association 1998;41(1):61-68
No abstract available.
Fever of Unknown Origin*
;
Fever*
2.Fever of unknown origin in children: A five-year review
Ma. Fema A. Cabanalan-Rivera ; Ma. Liza M. Antoinette M. Gonzales
Pediatric Infectious Disease Society of the Philippines Journal 2017;18(1):36-44
Objective:
The clinical presentation, outcome, and risk factors for mortality in children with Fever of Unknown Origin (FUO) were determined.
Methods:
Medical records of pediatric patients admitted for FUO from January 2009 to December 2013 were reviewed. Clinical manifestations, physical exam findings, diagnostic work-ups and final diagnosis were determined, as well as the relationship between final diagnosis and risk for mortality.
Results:
Fifty-seven patients with FUO were included. Weight loss, cough, colds, and rashes were common symptoms while pallor, lymphadenopathies, and hepatomegaly were common physical exam findings. All patients underwent Phase I evaluation for FUO, while 73.7% underwent further diagnostic tests. A specific etiology was established in 96.5% of cases: infectious, 43.9%, connective tissue disease, 38.6%, and hematologic/oncologic, 14%. Two cases remained to have no specific diagnosis. Majority of patients had a benign course and were discharged improved (84.2%). The mortality rate is 15.8% and was not associated with any disease category (p-value 0.204).
Conclusion
FUO in children occurs across all age groups. Its clinical presentations are varied and non-specific and common signs and symptoms are pallor, lymphadenopathies, weight loss, cough, colds. and joints pains. Infection is the most common cause of FUO in children, followed by connective tissue diseases and hematologic and oncologic diseases. The mortality rate from FUO is 15.8%.
Fever of Unknown Origin
3.Aortic dissection presenting as fever of unknown origin.
Su Nyoung CHOI ; Sung Ji PARK ; Tae Jung KWON ; Young Ran KANG ; So Ra PARK ; Chung Whan KWAK ; Jin Yong HWANG
Korean Journal of Medicine 2006;70(2):213-215
Aortic dissection most often presents with the severe chest pain and may have variable symptoms including fever. However, fever of unknown origin as the predominant manifestation of aortic dissection seems to be extremely rare. We report the case of a patient who sustained a prolonged spiking fever with unknown origin for 17 days following acute aortic dissection. The case serves as a reminder that prolonged fever may be the principal residual sequelae after aortic dissection.
Chest Pain
;
Fever of Unknown Origin*
;
Fever*
;
Humans
4.A Case of Pyogenic Liver Abscess with Fever of Unknown origin.
Soo Baeck LEE ; Kwang Soo HWANG ; Kyung Sook CHO ; Doo Sung MOON
Journal of the Korean Pediatric Society 1983;26(11):1145-1148
No abstract available.
Fever of Unknown Origin*
;
Fever*
;
Liver Abscess, Pyogenic*
5.Intravascular lymphoma of the inferior turbinate: An unusual rhinologic presentation of a rare neoplasm
Francis V Roasa ; Milabelle B Lingan
Philippine Journal of Otolaryngology Head and Neck Surgery 2007;22(1-2):24-26
Objective: To present a unique case of intravascular lymphoma of the inferior turbinate because of its rarity, unusual clinical presentation and difficulty in establishing a diagnosis. Design: Case Report Setting: A tertiary hospital Patient: A 66-year-old male admitted to the hospital due to intermittent high grade fever of six months duration. Result: The patient presented with fever of unknown origin, and exhaustive laboratory, ancillary procedures and biopsies to rule in/out infectious, autoimmune and oncologic causes were performed to arrive at a diagnosis. Nasal endoscopy revealed an enlarged, hypertrophied and violaceous right inferior turbinate with watery to mucoid discharge and septal deviation to the right confirmed by CT scans of the paranasal sinuses. Functional Endoscopic Sinus Surgery (FESS), septoplasty and turbinoplasty with biopsy revealed intravascular lymphoma. Chemotherapy was deferred due to the deteriorating medical condition and the patient expired seven months after the initial onset of symptoms. Conclusion: Patients who present with fever of unknown origin should undergo a thorough otorhinolaryngologic examination to exclude primary ENT conditions and ensure proper management. Given its rarity and multiplicity of presentation, it is extremely difficult to make a diagnosis of intravascular lymphoma. A high index of suspicion of intravascular lymphoma is necessary so that timely acquisition of tissue biopsy of any lesion involved will make a definite diagnosis. (Author)
LYMPHOMA FEVER FEVER OF UNKNOWN ORIGIN CASE REPORTS
6.The Cytopathology of Body Cavity Fluid.
Korean Journal of Cytopathology 2008;19(2):72-85
Cytologic examination of the body cavity fluid is very important because the specimens represent a significant percentage of nongynecologic samples and this cytologic examination may be the first, best or only chance for making the diagnosis of an underlying malignancy. The purposes of body cavity fluid examination are to correctly identify cancer cells and if possible, to identify the tumor types and primary sites when presented with unknown primary tumor sites. The most important basic differential diagnosis is that of benign and reactive disease vs malignant disease. Reactive mesothelial cells are a consistent population in body cavity fluid, and these are the most versatile cells in the body. Due to the specific environment of the body cavity, the exfoliated reactive mesothelial cells may show significant morphologic overlap with the morphology of cancer cells. With a focus on the differential points between reactive mesothelial cells and metastatic adenocarcinoma cells, the practical diagnostic approaches, the diagnostic clues and the pitfalls to achieve a correct diagnosis are presented in this review.
Adenocarcinoma
;
Diagnosis, Differential
;
Neoplasms, Unknown Primary
7.A Case of Relapsing Polychondritis Presented as Fever of Unknown Origin.
Ji Hyang KIM ; Suk Jin AHN ; Jin Seok KIM ; Hoon Suk CHA ; Jeong Ho HAN ; Eun Mi KOH ; Jae Hoon SONG
The Journal of the Korean Rheumatism Association 2000;7(1):62-66
Relapsing polychondritis is a rare autoimmune disease of unknown etiology with episodic but potentially progressive inflammatory manifestations. Auricular, articular and nasal manifestations are the most frequent disturbances. Fever is one of the manifestations of this disease but it rarely appears as an initial presentation. In this situation, the diagnosis is delayed until other manifestations are obvious. We report a case of relapsing polychondritis, which was presented as fever of unknown origin. Ten months after the onset of fever, auricular chondritis appeared and gave us the key to diagnosis.
Autoimmune Diseases
;
Diagnosis
;
Fever of Unknown Origin*
;
Fever*
;
Polychondritis, Relapsing*
8.Muscle tissue lymphoma presenting only with fever of unknown origin: a case report and literature review.
Xiaodong SHEN ; Xin CHEN ; Hongju XIAO ; Gang LIU ; Yongzhi ZHAI ; Baixuan XU ; Huaiyin SHI ; Tanshi LI ; Haiyan ZHU
Journal of Southern Medical University 2015;35(6):927-930
Extra-nodal malignant lymphoma is often characterized by a lack of typical symptoms and positive results of auxiliary examinations, which make diagnosis difficult. In some cases, fever can be the only clinical manifestation. For the lymphoma patients presenting with persistent fever with a duration over 3 weeks, characteristics of fever including time of fever attack, fever type and effects of drugs may have significant value in the diagnosis, especially in the early stage of the disease or in rare cases.
Fever of Unknown Origin
;
Humans
;
Lymphoma
;
diagnosis
;
Muscles
;
pathology
9.Ovarian Cancer That Was Initially Diagnosed as Malignant Pleural Effusion of Unknown Primary Origin
Toshihiko Fukuoka ; Eisuke Matsuoka ; Sahoko Chiba ; Satoshi Takayama ; Satoshi Ohno
Journal of Rural Medicine 2008;4(1):41-44
We report a case of adenocarcinoma detected in the right pleural effusion of a 75-year-old woman. Investigations failed to reveal the site of the primary lesion, and the case was treated as primary unknown cancer. The pleural effusion disappeared after chemotherapy; however, as there was serious bone marrow suppression, the clinical course was observed at an outpatient clinic without chemotherapy. A search for the primary lesion was repeated, but it was not found. One year after first admission, a chest X-ray showed left pleural effusion. Adenocarcinoma was detected in the effusion and a tumor mass obtained from the pleural cavity. Ovarian cancer was diagnosed based on the histological, serological and MRI findings. Thus, this was a rare case of ovarian cancer in which the diagnosis was confirmed by repeated evaluation and in which the initial diagnosis had been primary unknown cancer with malignant pleural effusion only.
Ovarian Cancer
;
Pleural Effusion, Malignant
;
Pleural Effusion
;
Unknown
;
Beginning
10.Multiple Chemical Sensitivity and Idiopathic Environmental Intolerance (Part One)
Mitsuyasu WATANABE ; Hideki TONORI ; Yoshiharu AIZAWA
Environmental Health and Preventive Medicine 2002;7(6):264-272
Multiple chemical sensitivity/idiopathic environmental intolerance (MCS/IEI) is a commonly used diagnostic term for a group of symptoms. These symptoms have been described and commented on for more than 15 years in the USA. Recently, it has also been observed in Japan. The main features of this syndrome are multiple symptoms involving in multiple organ systems that are precipitated by a variety of chemical substances with relapses and exacerbation under certain conditions when exposed to very low levels which do not affect the population at large. There are no laboratory markers or specific investigative findings. Although traditional medical organizations have not agreed on a definition for this syndrome due to the lack of obvious evidence to demonstrate the existence of these symptoms, it is being increasingly recognized. It constitutes an increasing percentage of the caseload at occupational/environmental medical clinics. Part one of this review article discusses pathophysiological theories, substances which cause symptoms, prevalence in the general and specific populations, past history and family history, and clinical symptoms of MCS/IEI patients.
symptoms <1>
;
Part
;
Intolerance, NOS
;
Unknown (origin)
;
Multiple Chemical Sensitivity