Rio de Janeiro, November 25th, 2018Dear EditorCryptococcosis can frequently complicate the course of the acquired immunodeficiency
syndrome, and cryptococcal meningoencephalitis is by far its main clinical presentation
. In fact, the organism is ubiquitous in soil and dust and is acquired by the
inhalation of infectious propagules from the environment
. Other sites of extraneural involvement include the joints, oral cavity,
pericardium, skin, mediastinum and genitourinary tract
.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
,
. 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 AIDSpatient 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.
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”
, “epigastric abdominal pain and biliary vomiting”
, “odynophagia and intractable vomiting”
, “acute worsening of chronic watery diarrhea with melena”
and “chronic dysphagia with epigastralgia”
.Intraabdominal cryptococcosis at sites other than the stomach has been reported in the
esophagus, duodenum, jejunum, ileum, colon and the gallbladder
,
-
. It may present as cryptococcal peritonitis
, as an acute abdomen due to jejunal perforation
, as an acute appendicitis in a case of mesenteric cryptococcal lymphadenitis
, as epigastric discomfort, early satiety and abdominal distention in a case of
duodenal cryptoccoccosis
, and as a retroperitoneal cryptococcoma mimicking a pancreatic tumor
.Endoscopic and macroscopic pathologic findings of gastric cryptococcosis have been
described as lesions of yellowish granular appearance
, as nodules
, as nodules with central erosions resembling inflammatory polyps
, as a circumscribed lesion with central umbilication
, as circumscribed nodules, some having central erosions resembling inflammatory
polyps
, as irregular gastric ulcers, occasionally with red-pigmented lesions within
the ulcer
and as gastric erosions
.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 .
reported the case of a 37 year-old HIV-infectedman 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
. Moreover, Ferraioli et al .
reported the case of a 50-year-old HIV-infectedwoman 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. AIDSpatients with gastrointestinal
cryptococcosis generally have an exceedingly low CD4 cell count. Most reported cases had
less than 50 CD4 cells/mm
,
-
,
and concomitant cryptococcal meningoencephalitis is also common
,
-
,
,
, but some patients apparently had no evidence of neurologic disease
,
,
. Esophagogastroduodenoscopy followed by histopathology of biopsy samples have
proved to be an invaluable diagnostic tool
-
,
.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 AIDSpatients.