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1,970 Possible Causes for Fever, Hepatosplenomegaly

  • Infectious Mononucleosis

    Both cases involved young adults presenting with fever, pharyngitis, lymphadenopathy, hepatosplenomegaly, and atypical lymphocytosis confirmed by serologic tests, liver biopsy[] Glandular fever mostly affects teenagers and young adults.[] She presented with fever, skin rash, lymphadenopathy, and hepatosplenomegaly.[]

  • Pharyngitis

    Presence of hepatosplenomegaly or lymphadenopathy outside the cervical region should raise suspicions regarding an underlying malignancy.[] Most of these children have undergone workup(s) for sepsis performed by their pediatricians because of the associated high fever.[] Abdomen: Hepatosplenomegaly can be found in infectious mononucleosis infection.[]

  • Otitis Media

    Bowel sounds present in all 4 quadrants, no hepatosplenomegaly MSK: Full range of motion in all extremeties Comparing the left and right sides of the ear helps in pinpointing[] If your child is younger than three months of age and has a fever, it’s important to always call your healthcare provider right away.[] […] the following: Labyrinthitis - Fever, nystagmus, serous or suppurative otitis media Mastoiditis with subperiosteal abscess - Fever, fluctuance overlying the mastoid area,[]

  • Insect Bite

    A condition mainly seen in Japanese children, in which a mosquito bite is followed by local skin necrosis combined with fever, lymphadenopathy, and hepatosplenomegaly ( 21[] Rocky Mountain Spotted Fever Rocky Mountain Spotted Fever is caused by bacterium Rickettsia rickettsii that is transmitted by infected ixodid (hard) ticks.[] They serve as vectors for viruses (e.g., those viruses causing yellow fever, Dengue fever, West Nile fever), bacteria (mainly Enterobacteriaceae) and protozoa (e.g., Dirofilaria[]

  • Adult-Onset Still Disease

    Other common manifestations of AOSD are lymphadenopathy, hepatosplenomegaly, muscle aches, and pharyngitis.[] Intense pruritus and linear erythematous lesions flared with a spiking fever, usually in the late afternoon and evening.[] Adult onset Still's disease (AOSD) is a systemic inflammatory disease characterized by high-fevers, articular involvement, maculopapular rash, hepatosplenomegaly, lymphadenopathy[]

  • Malignant Histiocytosis

    Abstract A 70-year-old woman was admitted for evaluation of hepatosplenomegaly, fever and elevated serum LDH levels.[] Abstract A 10-year-old boy with malignant histiocytosis presented with fever, hepatosplenomegaly, and diffuse pancreatic enlargement, mimicking acute pancreatitis.[] This is clearly seen in the seven patients we report where the initial diagnoses were that of viral fever or hepatitis.[]

  • Hepatosplenic T-cell Lymphoma

    Abstract We report a case of a man presenting with an unexplained fever, pancytopenia and hepatosplenomegaly without lymphadenopathy.[] The authors report the case of a young immunocompetent man, who was admitted to the hospital with a history of prolonged, unexplained fever, fatigue and weight loss.[] The patient complained of fever and heaviness of left upper abdomen.[]

  • Juvenile Onset Stills Disease

    Appearance of rash, hepatosplenomegaly, serositis and generalized lymphadenopathy.[] This characteristic diagnostic triad may also be associated with an adenopathy and hepatosplenomegaly.[] Still's Disease Symptoms Fever Fever is part of the body's own disease-fighting arsenal.[]

  • Visceral Leishmaniasis

    The infant suffered from intermittent fever for 5 weeks, and hepatosplenomegaly and pancytopenia, and was successfully treated with a short course of liposomal amphotericin[] Surprisingly, fever started after beginning of meglumine antimoniate treatment in this patient.[] Infection is characterized by pancytopenia (anemia, thrombocytopenia, neutropenia), hepatosplenomegaly, fever, and severe immunosuppression that can lead to fatal opportunistic[]

  • Angioimmunoblastic Lymphadenopathy

    AILD is characterized by generalized lymphadenopathy, hepatosplenomegaly, immunological abnormalities, polyclonal hypergammaglobulinemia and anemia.[] Although complete remission of AML was achieved, fever persisted and atypical skin rash followed by generalized lymphadenopathy along with polyclonal hypergammaglobulinemia[] Angioimmunoblastic lymphadenopathy with disproteinemia (AILD) is a systemic lymphoproliferative disorder characterized by constitutional symptoms such as generalized lymphadenopathy, hepatosplenomegaly[]

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