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splenomegaly/gorączka

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BACKGROUND Cardiovascular parameters can be impaired by repeated infections with P. falciparum. This study aimed at investigating the influence of gametocyte carriage on; the prevalence of fever and splenomegaly, blood pressure, heart rate and haematological indices in children <15 years, in the

["Peculiar infection" with fever, splenomegaly and acute kidney failure in a 24-year-old forestry student].

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When confronted by the combination of initial high fever associated with intense malaise, splenomegaly, elevated levels of transaminases, and acute renal failure, consideration must be given to the differential diagnosis of leptospirosis even in Germany. As a rule, the diagnosis is confirmed by

Kikuchi's necrotizing lymphadenitis: a cause of fever of unknown origin and splenomegaly.

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Kikuchi's disease is characterized by lymphadenopathy in young patients and may be mistaken for malignant disease both clinically and histologically. We report the case of a 26-year-old man with persistent fever for 3 weeks and splenomegaly, in whom pancytopenia developed afterwards. A bone marrow

A case of periodic fever and persistent splenomegaly in a 2-year-old boy.

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We report an unusual case of periodic fever associated with persistent splenomegaly in a 2-year-old boy. Febrile episodes occurred at regular 2 weekly intervals and each lasted for 1-2 days. Following resolution of the fever on each occasion, the patient developed neck stiffness of 1-2 days

Hyper-reactive malarial splenomegaly: rare cause of pyrexia of unknown origin.

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Hyper-reactive malarial splenomegaly (HMS) or Tropical splenomegaly syndrome(TSS), occurs in areas of high transmission of malaria. These children usually presents with gross splenomegaly and abdominal discomfort, while fever is not the usual manifestation in majority of them. It is a disease of

Diagnostic splenectomy in patients with fever of unknown origin and splenomegaly.

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OBJECTIVE To review the diagnostic significance, safety and possible risk factors of splenectomy in fever of unknown origin (FUO) with splenomegaly. METHODS The records of 54 patients with FUO and splenomegaly who underwent splenectomy in our hospital in the past 20 years were reviewed
BACKGROUND We reviewed patients with fever of unknown origin (FUO) and splenomegaly and assessed the diagnostic value of splenectomy and measured risk factors suggestive of an underlying lymphoma. METHODS FUO patients (n = 83) who had splenomegaly and underwent splenectomy were enrolled into this

[Visceral leishmaniasis as a rare cause of a fever of unknown origin associated with splenomegaly].

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We present a case of a 22-year-old man admitted to the hospital because of prolonged fever associated with splenomegaly. During the previous 2 years the patient spent several months as a manual worker in the south of Italy. Manifestations of the disease included progressive weight loss,

[Polyarthralgia, fever and purpura in a patient known to have splenomegaly].

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A 43-year-old patient was admitted for swollen and painful ankles, knees and elbows, palpable purpura of the lower extremities and fever. Splenomegaly had been diagnosed 5 years previously. At clinical workup, spleen and liver size were increased and purplish papular skin lesions were noted above

A rare presentation of visceral leishmaniasis without fever or splenomegaly in an elderly person.

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Visceral leishmaniasis (kala azar) is characterized by fever and splenomegaly in more than 80% of cases. We report a case of kala azar in an elderly person with severe anemia but no other typical features. This highlights the importance of being aware of rare presentations to avoid missing the

[Fever, pancytopenia, and splenomegaly 8 months after a trip to Majorca Island (Spain)].

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BACKGROUND Visceral leishmaniasis is a rare imported infectious disease in Germany. Approximately ten to 30 cases are recorded annually. The classic symptoms are often misinterpreted as lymphoma of the spleen. METHODS A 46-year-old patient presented with fever, malaise, night sweats, pancytopenia,

The First Case of Adult-Onset Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenitis Syndrome with Splenomegaly in Iran.

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Periodic fever, aphthous stomatitis, pharyngitis, and adenitis syndrome (PFAPA) is an auto-immune based disease known as a syndrome for pediatrics which typically occurs in children ≤ 5 years of age, but in 2008, for the first time, one adult case of this disease was

An 8-Year-Old Boy With Fever, Splenomegaly, and Pancytopenia

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An 8-year-old boy with no significant past medical history presented to his pediatrician with 5 days of fever, diffuse abdominal pain, and pallor. The pediatrician referred the patient to the emergency department (ED), out of concern for possible malignancy. Initial vital signs indicated fever,

Pel-Ebstein fever coinciding with cyclical haemolytic anaemia and splenomegaly in a patient with Hodgkin's disease.

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A 46-year-old man with an aortic valve replacement was investigated for recurrent episodes of fever associated with splenomegaly and haemolytic anaemia. Initially bacterial endocarditis was suspected. At laparotomy he proved to have mixed cellularity Hodgkin's disease confined to the spleen. The

Prolonged intermittent fever and massive splenomegaly in a miner working in the tropical jungle, China

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Prolonged fever is a particular challenge. A 47-year-old man with 5-year intermittent fever and remarkable splenomegaly was diagnosed as chronic melioidosis after splenectomy. The case would help clinicians to raise awareness and include chronic melioidosis in the differential diagnosis for patients
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