Gastric cryptococcosis

an unusual presentation of a common opportunistic disorder

  • Walter de Araujo Eyer-Silva Universidade Federal do Estado do Rio de Janeiro, Centro de Ciências Biológicas e da Saúde, Hospital Universitário Gaffrée e Guinle
  • Thaynny Cândida de Oliveira Universidade Federal do Estado do Rio de Janeiro, Centro de Ciências Biológicas e da Saúde, Hospital Universitário Gaffrée e Guinle
  • Ricardo de Souza Carvalho Universidade Federal do Estado do Rio de Janeiro, Centro de Ciências Biológicas e da Saúde, Hospital Universitário Gaffrée e Guinle
  • Isabelle de Carvalho-Rangel Universidade Federal do Estado do Rio de Janeiro, Centro de Ciências Biológicas e da Saúde, Hospital Universitário Gaffrée e Guinle
  • Rodrigo Panno Basílio-de-Oliveira Universidade Federal do Estado do Rio de Janeiro, Centro de Ciências Biológicas e da Saúde, Hospital Universitário Gaffrée e Guinle, Serviço de Anatomia Patológica
  • Luciana Ferreira de Araujo Universidade Federal do Estado do Rio de Janeiro, Centro de Ciências Biológicas e da Saúde, Hospital Universitário Gaffrée e Guinle, Serviço de Anatomia Patológica
  • Guilherme Almeida Rosa da Silva Universidade Federal do Estado do Rio de Janeiro, Centro de Ciências Biológicas e da Saúde, Hospital Universitário Gaffrée e Guinle
  • Rogério Neves-Motta Universidade Federal do Estado do Rio de Janeiro, Centro de Ciências Biológicas e da Saúde, Hospital Universitário Gaffrée e Guinle

Abstract

 

 

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Published
2019-02-07
How to Cite
Eyer-Silva, W., Oliveira, T., Carvalho, R., Carvalho-Rangel, I., Basílio-de-Oliveira, R., Araujo, L., Silva, G., & Neves-Motta, R. (2019). Gastric cryptococcosis. Revista Do Instituto De Medicina Tropical De São Paulo, 61, e10. https://doi.org/10.1590/S1678-9946201961010
Section
Letter to the Editor

Rio de Janeiro, November 25th, 2018

Dear Editor

Cryptococcosis can frequently complicate the course of the acquired immunodeficiency syndrome, and cryptococcal meningoencephalitis is by far its main clinical presentation 1 . In fact, the organism is ubiquitous in soil and dust and is acquired by the inhalation of infectious propagules from the environment 1 . Other sites of extraneural involvement include the joints, oral cavity, pericardium, skin, mediastinum and genitourinary tract 1 .

The stomach is rarely the site of an opportunistic infection so that gastric cryptococcosis is an extremely rare complication. However, it may be the first clinical presentation of AIDS 2,3 . Gastric or gastrointestinal cryptococcosis may be clinically silent or present with nonspecific symptoms frequently attributable to other more prevalent disorders. We present a case of gastric cryptococcosis in an AIDS patient who had concomitant cryptococcal meningoencephalitis and disseminated Kaposi’s sarcoma.

A 34 year-old African-Brazilian male patient presented with a 2-month history of epigastralgia, nauseas and vomiting that progressed within a few weeks to persistent headaches. The patient had a diagnosis of HIV infection made 6 years before and was non-adherent to the antiretroviral treatment. Within the last few months, multiple cutaneous lesions of Kaposi’s sarcoma had developed (confirmed by biopsy). The CD4 cell count was 10/mm3 and the plasma HIV viral load was 74,411 copies/mL (4.8 log). Cerebrospinal fluid examination yielded a diagnosis of cryptococcal meningitis through direct examination and fungal culture. Esophagogastroduodenoscopy disclosed raised reddened lesions over the body of the stomach, some of which had a central ulceration. There were also two reddened, flattened lesions in the antrum and one lesion in gastric fundus. Histopathologic analyses of biopsy samples revealed a diagnosis of gastric cryptococcosis ( Figure 1 ). There was no histopathological evidence of gastric Kaposi’s sarcoma. Treatment was initiated with amphotericin B deoxycholate, as well as prophylaxis of other opportunistic infections, but the patient eventually died of respiratory failure four weeks after admission.

A) Hematoxylin and eosin staining (original magnification 200 x) discloses oxyntic glands in the body of the stomach with marked edema and a lymphoplasmacytic inflammatory reaction of the lamina propria. Extracellular varied-sized round structures with a halo clearing around each organism are seen (black circles); B) Grocott methenamine silver (GMS) staining (original magnification 200 x) unmasks variable-sized yeast-like structures (red circle); C) Higher resolution (original magnification 400 x) GMS staining shows some organisms with a narrow-based budding (arrow) consistent with Cryptococcus spp.

Figure 1: A) Hematoxylin and eosin staining (original magnification 200 x) discloses oxyntic glands in the body of the stomach with marked edema and a lymphoplasmacytic inflammatory reaction of the lamina propria. Extracellular varied-sized round structures with a halo clearing around each organism are seen (black circles); B) Grocott methenamine silver (GMS) staining (original magnification 200 x) unmasks variable-sized yeast-like structures (red circle); C) Higher resolution (original magnification 400 x) GMS staining shows some organisms with a narrow-based budding (arrow) consistent with Cryptococcus spp.

The clinical presentation of gastric cryptococcosis has been described as symptoms of “gastroesophageal reflux including odynophagia” 4 , “epigastric abdominal pain and biliary vomiting” 5 , “odynophagia and intractable vomiting” 3 , “acute worsening of chronic watery diarrhea with melena” 6 and “chronic dysphagia with epigastralgia” 7 .

Intraabdominal cryptococcosis at sites other than the stomach has been reported in the esophagus, duodenum, jejunum, ileum, colon and the gallbladder 4,8-12 . It may present as cryptococcal peritonitis 8 , as an acute abdomen due to jejunal perforation 9 , as an acute appendicitis in a case of mesenteric cryptococcal lymphadenitis 10 , as epigastric discomfort, early satiety and abdominal distention in a case of duodenal cryptoccoccosis 11 , and as a retroperitoneal cryptococcoma mimicking a pancreatic tumor 12 .

Endoscopic and macroscopic pathologic findings of gastric cryptococcosis have been described as lesions of yellowish granular appearance 13 , as nodules 4 , as nodules with central erosions resembling inflammatory polyps 2 , as a circumscribed lesion with central umbilication 2 , as circumscribed nodules, some having central erosions resembling inflammatory polyps 2 , as irregular gastric ulcers, occasionally with red-pigmented lesions within the ulcer 6 and as gastric erosions 3 .

It has also been suggested that some cases of gastrointestinal cryptococcosis may be a manifestation of the immune reconstitution inflammatory syndrome (IRIS). Musubire et al . 14 reported the case of a 37 year-old HIV-infected man with a history of cryptococcal meningitis who presented with subacute, worsening abdominal pain and abdominal lymphadenopathy during immune recovery. He was initially treated for presumed abdominal tuberculosis, but subsequently developed a perforation of the ileum requiring bowel resection. Histopathology confirmed a cryptococcoma of the ileum 14 . Moreover, Ferraioli et al . 12 reported the case of a 50-year-old HIV-infected woman who presented with low-grade fever and abdominal pain due to a retroperitoneal cryptococcoma 15 months after being diagnosed with cryptococcal meningitis.

Our patient had a very low CD4 cell count and developed gastric cryptococcosis associated with cryptococcal meningoencephalitis. AIDS patients with gastrointestinal cryptococcosis generally have an exceedingly low CD4 cell count. Most reported cases had less than 50 CD4 cells/mm 3 3,10-12,14 and concomitant cryptococcal meningoencephalitis is also common 2,5-7,10,11 , but some patients apparently had no evidence of neurologic disease 3,8,9 . Esophagogastroduodenoscopy followed by histopathology of biopsy samples have proved to be an invaluable diagnostic tool 2-7,11 .

In summary, gastric and gastrointestinal cryptococcosis is generally a complication of advanced AIDS in patients with severe CD4 cell depletion. It may present as an acute abdominal episode or with nonspecific chronic symptoms. Therefore, it requires a high index of suspicion. Endoscopic studies and appropriate histopathological analyses are of utmost importance to the diagnosis. The present case seems to emphasize that physicians should constantly exercise a high index of suspicion of uncommon presentations of common opportunistic infections in AIDS patients.

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