Literature DB >> 20682856

Colonic leishmaniasis followed by liver transplantation.

Stanley Almeida Araujo1, Thaís Costa Nascentes Queiroz, Monica Maria Demas Alvares Cabral.   

Abstract

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Year:  2010        PMID: 20682856      PMCID: PMC2911159          DOI: 10.4269/ajtmh.2010.09-0430

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


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A 17-year-old, 37-kg Brazilian man was diagnosed with autoimmune hepatitis at the age of 7 years and underwent liver transplant (cadaveric) at the age of 14. Immunosuppressants included tacrolimus and prednisone. He had lost 3 kg over the previous year and had diarrhea with blood streaks in the previous 3 months but no history of fever. Laboratory tests showed pancytopenia (hemoglobin = 8.1 g/dL; leukocytes = 1,300/mm3; platelets = 79,000/mm3; albumin = 2.7 g/dL). Physical examination showed enlarged liver and spleen. Unrevealing imaging included upper gastroenterointestinal endoscopy, abdominal ultrasound, and computerized tomography of the chest and abdomen (Figure 1) but showed hepatosplenomegaly. Viral serologies were negative. Colonoscopy showed gross nodularity, hyperemia, and friability of the colonic mucosa (Figure 2). Biopsy of terminal ileum region showed amastigote forms of Leishmania inside macrophages (Figure 3A and B). The nature of the agent was confirmed by immunohistochemistry (Figure 3C) and polymerase chain reaction (PCR), which showed L. chagasi infection.1 Examination of a bone-marrow biopsy showed innumerable Leishmania amastigotes (Figure 3D). Serology for leishmaniasis was negative. Treatment with amphotericin B desoxycholate was initiated; renal function deteriorated, and treatment with liposomal amphotericin was substituted (3 mg/kg for 7 days).2 The patient clinically responded with resolution of diarrhea, weight gain, and normalization of spleen size. Two months later, hemoglobin was 11.3 g/dL, leukocytes were 3,670/mm3, platelets were 164,000/mm3, and albumin was 3.8 g/dL.1,2
Figure 1.

Computerized tomography of the abdomen showing hepatosplenomegaly.

Figure 2.

Colonoscopic view—irregular nodularity and hyperemia of the mucosa. This figure appears in color at www.ajtmh.org.

Figure 3.

Biopsy of colon and bone marrow. (A) Increased cellularity of the colon because of mononuclear inflammatory infiltrate. (B) Detail shows macrophages filled with amastigote forms of Leishmania chagasi. (C) Positive immunohistochemical reaction by the streptavidin-biotin method, with specific staining of the amastigotes. (D) Amastigote-parasitized macrophage in bone-marrow aspirate. This figure appears in color at www.ajtmh.org.

Computerized tomography of the abdomen showing hepatosplenomegaly. Colonoscopic view—irregular nodularity and hyperemia of the mucosa. This figure appears in color at www.ajtmh.org. Biopsy of colon and bone marrow. (A) Increased cellularity of the colon because of mononuclear inflammatory infiltrate. (B) Detail shows macrophages filled with amastigote forms of Leishmania chagasi. (C) Positive immunohistochemical reaction by the streptavidin-biotin method, with specific staining of the amastigotes. (D) Amastigote-parasitized macrophage in bone-marrow aspirate. This figure appears in color at www.ajtmh.org.
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Review 1.  Leishmaniasis: recognition and management with a focus on the immunocompromised patient.

Authors:  Christine M Choi; Ethan A Lerner
Journal:  Am J Clin Dermatol       Date:  2002       Impact factor: 7.403

2.  An alternative immunohistochemical method for detecting Leishmania amastigotes in paraffin-embedded canine tissues.

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Journal:  J Immunol Methods       Date:  2004-09       Impact factor: 2.303

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1.  Transplantation in the tropics: lessons on prevention and management of tropical infectious diseases.

Authors:  Ligia C Pierrotti; Camille N Kotton
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2.  New challenges in the epidemiology and treatment of visceral leishmaniasis in periurban areas.

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Review 3.  Histologic features of colonic infections.

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Review 4.  New insights into leishmaniasis in the immunosuppressed.

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Journal:  PLoS Negl Trop Dis       Date:  2018-05-10
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