Literature DB >> 32099811

Hidden disseminated extracutaneous AIDS-related Kaposi sarcoma.

Naoki Kawakami1, Ho Namkoong2,3, Masayuki Shimoda4, Hiroshi Kotani5,6, Hiroshi Fujiwara5, Naoki Hasegawa5.   

Abstract

A 68-year-old man with past medical history of multiple cerebral infarctions presented to our hospital with subacute paresis. His vital signs on presentation were normal, and his physical examination, other than his neurological findings, was unremarkable. Neurological examinations suggested cerebellar ataxia. Laboratory testing confirmed positive for human immunodeficiency virus (HIV) infection. His CD4-positive lymphocyte count was 45/μL, and HIV-RNA was 2.3 × 105 copies/mL. Brain computed tomography (CT) scan revealed multiple mass lesions and brain magnetic resonance imaging (MRI) with fluid-attenuated inversion-recovery (FLAIR) revealed periventricular hyperintensities, which suggested multiple malignant lymphoma and HIV encephalopathy. His state of consciousness had gradually worsened. Eventually, he died one month after admission. The autopsy unexpectedly showed disseminated Kaposi's sarcoma (KS). KS lesions were found in the stomach, small intestine, liver, spleen, mesentery and lungs. KS was not observed on his skin. Gross findings revealed multiple nodular lesions in each organ, and hematoxylin and eosin staining showed proliferation of spindle cells with vascular proliferation. Immunostaining was positive both for endothelial marker (CD31 and von Willebrand factor) and lymphatic endothelial marker (D2-40), which were consistent with KS.KS is the most common tumor in AIDS patients. It is caused by the human herpes-virus 8 infection. It manifests an indolent clinical course and mostly involves cutaneous lesions over the lower limbs, trunk and oral cavity. In this case, autopsy revealed disseminated KS pathologically, which was unrecognized before his death. This case highlights the possible existence of disseminated KS even without its cutaneous findings.
© 2020 The Authors. Published by Elsevier Ltd.

Entities:  

Keywords:  Acquired immune deficiency syndrome (AIDS); Disseminated Kaposi Sarcoma (KS); Human immunodeficiency virus (HIV)

Year:  2020        PMID: 32099811      PMCID: PMC7030992          DOI: 10.1016/j.idcr.2020.e00716

Source DB:  PubMed          Journal:  IDCases        ISSN: 2214-2509


Case illustrated

A 68-year-old man, a former smoker, with past medical history of multiple cerebral infarctions presented to our hospital with subacute paresis. He was a man who had sex with men (MSM). His vital signs on presentation were normal, and his physical examination, other than his neurological findings, was unremarkable. Neurological examination suggested cerebellar ataxia. Laboratory testing was positive for human immunodeficiency virus (HIV) infection. His CD4-positive lymphocyte count was 45/μL, and HIV-RNA was 2.3×105 copies/mL. Brain computed tomography (CT) scan revealed multiple mass lesions and brain magnetic resonance imaging (MRI) with fluid-attenuated inversion-recovery (FLAIR) revealed periventricular hyperintensities, which in addition to cerebral infarction, suggested multiple malignant lymphoma or HIV encephalopathy. Even with the initiation of anti-retroviral therapy (ART), his level of consciousness had gradually worsened along with acute gastrointestinal bleeding. One month after admission, the patient died due to pneumonia. The autopsy unexpectedly showed disseminated Kaposi sarcoma (KS), in addition to HIV encephalopathy and multiple central nervous system diffuse large B-cell lymphoma. KS lesions were found in the stomach, small intestine, liver, spleen, mesentery and lungs (Fig. 1). However, KS was not observed on his skin. Gross findings revealed multiple nodular lesions in the affected organs, and hematoxylin and eosin staining showed proliferation of spindle cells with vascular proliferation (Fig. 1). Immunostaining was positive for endothelial markers (CD31 and von Willebrand factor) and lymphatic endothelial marker (D2-40), which are consistent with KS (Fig. 2).
Fig. 1

A: Gross findings of the small intestine and mesentery showing nodular lesions (black arrow), B (low magnification) and C (high magnification): HE staining of the small intestine and mesentery showing nodular lesions from the submucosa to serosal layer, D: Gross findings of the liver showing diffuse nodular lesions (black arrow), E: HE staining of the liver showing proliferation of blood vessels and spindle cells (low magnification), F: Gross findings of the lung showing nodular lesions (white arrow), G: HE staining of the lung showing proliferation of spindle cells (low magnification), H: Gross findings of the stomach showing nodular lesions (white arrow), I: HE staining of the stomach showing proliferation of spindle cells in the stomach wall (low magnification).

Fig. 2

A: Immuno-staining for von Willebrand factor showing positive findings, B: Immunostaining for CD31 showing positive findings, C: Immunostaining for D2-40 showing positive findings. HE: Hematoxylin and eosin.

A: Gross findings of the small intestine and mesentery showing nodular lesions (black arrow), B (low magnification) and C (high magnification): HE staining of the small intestine and mesentery showing nodular lesions from the submucosa to serosal layer, D: Gross findings of the liver showing diffuse nodular lesions (black arrow), E: HE staining of the liver showing proliferation of blood vessels and spindle cells (low magnification), F: Gross findings of the lung showing nodular lesions (white arrow), G: HE staining of the lung showing proliferation of spindle cells (low magnification), H: Gross findings of the stomach showing nodular lesions (white arrow), I: HE staining of the stomach showing proliferation of spindle cells in the stomach wall (low magnification). A: Immuno-staining for von Willebrand factor showing positive findings, B: Immunostaining for CD31 showing positive findings, C: Immunostaining for D2-40 showing positive findings. HE: Hematoxylin and eosin. KS is the most common tumor in patients with acquired immunodeficiency syndrome (AIDS), especially in MSM. KS is caused by the human herpes-virus 8 infection [1]. It has an indolent clinical course and mostly involves cutaneous lesions over the lower limbs, trunk, and oral cavity [2]. In this case, autopsy revealed disseminated KS, which was unrecognized before his death. The gastrointestinal bleeding might be related to his gastrointestinal KS. We were unable to perform endoscopy for gastrointestinal bleeding due to his worsening clinical status. This case highlights the possibility of disseminated KS being present even in the absence of cutaneous lesions.

Funding statement

The authors have no funding to report.

Informed consent

Written informed consent was unobtainable because the patient was deceased.

CRediT authorship contribution statement

Naoki Kawakami: Writing - original draft. Ho Namkoong: Conceptualization, Data curation, Project administration, Supervision, Writing - original draft, Writing - review & editing. Masayuki Shimoda: Data curation, Writing - review & editing. Hiroshi Kotani: Data curation, Writing - review & editing. Hiroshi Fujiwara: Data curation, Writing - review & editing. Naoki Hasegawa: Supervision, Writing - review & editing.

Declaration of Competing Interests

The authors have declared that no competing interests exist.
  2 in total

Review 1.  Kaposi Sarcoma Updates.

Authors:  Shervin A Etemad; Anna K Dewan
Journal:  Dermatol Clin       Date:  2019-07-10       Impact factor: 3.478

Review 2.  Kaposi sarcoma.

Authors:  Ethel Cesarman; Blossom Damania; Susan E Krown; Jeffrey Martin; Mark Bower; Denise Whitby
Journal:  Nat Rev Dis Primers       Date:  2019-01-31       Impact factor: 52.329

  2 in total

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