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            <title><![CDATA[Rabies encephalitis in a preschool child following postexposure prophylaxis]]></title>
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            <link>https://www.novareader.co/book/isbn/10.1371/journal.pntd.0009045</link>
            <description><![CDATA[<p class="para" id="N65542">We report a case of rabies encephalitis in a 4½-year-old male child with an exposure to a suspect rabid dog. The child developed rabies 25 days after receiving postexposure prophylaxis. Rabies immunoglobulin (RIG) is currently administered according to body weight. In high-risk exposures over the head and neck, local administration of RIG over and above the body weight depending on the site, size, and severity of exposure may help to prevent rabies death. There is a need for further studies to generate new evidence in this regard.</p>]]></description>
            <pubDate><![CDATA[2021-02-18T00:00]]></pubDate>
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            <title><![CDATA[Skin maculae, chronic diarrhea, cachexia, and splenomegaly—Late presentation of the first autochthonous case of visceral leishmaniasis in Tanzania]]></title>
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            <link>https://www.novareader.co/book/isbn/10.1371/journal.pntd.0008925</link>
            <description><![CDATA[<p class="para" id="N65539">A 20-year-old man from Simanjiro district in northern Tanzania presented with a 3-year history of splenomegaly, fatigue, cachexia, skin maculae, and recent onset of watery diarrhea at Kilimanjaro Christian Medical Centre (KCMC) in Northern Tanzania. Due to laboratory findings of pancytopenia, diagnostic workup included bone marrow aspiration cytology and biopsy. Although the rapid test (IT LEISH, rK39 RDT) was negative, blood smear showed amastigote forms of leishmaniasis in macrophages. Repeat bone marrow aspiration and PCR eventually confirmed visceral leishmaniasis (VL). The patient denied travel to known endemic areas of VL. Treatment was initiated with Amphotericin B, but the patient died on the fourth day of treatment from respiratory insufficiency. An autopsy revealed massive organ manifestations of VL. This is the first reported autochthonous case of VL in Tanzania. Clark and colleagues detected the vector <i>Phlebotomus martini</i> in Northern Tanzania in 2013, in a region bordering the district of our patient. The negative rapid test draws attention to the fact that sensitivity and specificity were found to be low in East African VL patients as displayed earlier by a Kenyan study. Therefore, tissue samples (spleen or bone marrow) remain necessary for diagnosis. The variety of symptoms in this presented case was remarkable, including the occurrence of post-kala-azar dermal leishmaniasis (PKDL) and VL at the same time. This has been described in East African VL cases before as well as the occurrence of chronic diarrhea. An elongated undiagnosed period likely led to a mixed clinical picture that included hepato-splenomegaly, PKDL, cachexia, and diarrhea.</p>]]></description>
            <pubDate><![CDATA[2021-01-14T00:00]]></pubDate>
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            <title><![CDATA[Challenges in establishing telehealth care during the COVID-19 pandemic in a neglected HTLV-1-infected population in northeastern Brazil]]></title>
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            <link>https://www.novareader.co/book/isbn/10.1371/journal.pntd.0008922</link>
            <description><![CDATA[]]></description>
            <pubDate><![CDATA[2020-12-31T00:00]]></pubDate>
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