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Primary gastric actinomycosis: report of a case diagnosed in a gastroscopic biopsy
© Al-Obaidy et al.; licensee BioMed Central. 2015
Received: 7 April 2014
Accepted: 9 February 2015
Published: 26 February 2015
Primary gastric actinomycosis is extremely rare, the appendix and ileocecal region being the most commonly involved sites in abdominopelvic actinomycosis. Herein, we report a case of primary gastric actinomycosis. The diagnosis was made on microscopic evaluation of gastroscopic biopsy specimens. To the best of our knowledge, this is the third case to be reported in the literature, in which the diagnosis was made in a gastroscopic biopsy rather than a resection specimen.
An 87-year-old Saudi male on medication for cardiomyopathy, premature ventricular contractions, renal impairment, hypertension, and dyslipidemia, presented to the emergency department with acute diffuse abdominal pain, abdominal distension, constipation and vomiting for two days, with no history of fever, abdominal surgery or trauma. The patient was admitted to the hospital with an impression of gastric outlet obstruction. Based on radiologic and gastroscopic findings, a non-infectious etiology was suspected, possibly adenocarcinoma or lymphoma. Gastroscopic biopsies showed an actively inflamed, focally ulcerated atrophic fundic mucosa along with fragments of a fibrinopurulent exudate containing brownish, iron negative pigment and abundant filamentous bacteria, morphologically consistent with Actinomyces.
Althuogh extremely rare, primary gastric actinomycosis should be considered in the differential diagnosis of radiologic and gastroscopic diffuse gastric wall thickening and submucosal tumor-like or infiltrative lesions, particularly in patients with history of abdominal surgery or trauma, or those receiving extensive medication. A high level of suspicion is required by the pathologist to achieve diagnosis in gastroscopic biopsies. Subtle changes such as the presence of a pigmented inflammatory exudate should alert the pathologist to perform appropriate special stains to reveal the causative organism.
KeywordsActinomycosis Gastric Grocott’s Gram PAS
Actinomycosis is a chronic suppurative granulomatous inflammation caused by anaerobic, filamentous, Gram-positive bacteria of Actinomyces species, most often Actinomyces israelii. There are three main forms of actinomycosis, namely, cervicofacial (31%-65%), abdominopelvic (20%-36%) and thoracic (15%-30%) [1-4]. In abdominopelvic actinomycosis, the appendix and ileocecal region are the most commonly involved sites (65%) [2,3,5-7]. Primary gastric actinomycosis is extremely rare, with only 23 cases reported to date [5,6,8-20]. Herein, we report a case of primary gastric actinomycosis. The diagnosis was made on microscopic evaluation of gastroscopic biopsy specimens. To the best of our knowledge, this is the third case to be reported in the literature, in which the diagnosis was made in a gastroscopic biopsy rather than a resection specimen [6,8].
Clinical and laboratory findings
The patient was then managed conservatively in the hospital. A third gastroscopic biopsy two weeks later revealed chronic atrophic gastritis with no Actinomyces detected, and the patient appeared in a good health status. A plan was set up to start him on the appropriate antibiotic therapy for actinomycosis with follow up gastroscopy after one month. However, the patient chose to continue treatment somewhere else. So he was discharged on his request and never showed up again in our institution.
Actinomycosis in human is most commonly caused by Actinomyces israelii [1,3,21-26] which is an endogenous commensal present in the oral and GI-tract flora [9,10,12,22,27]. Actinomycetes typically invade injured mucosa with opportunistic infection occuring if there is a break in the mucosal barrier. Factors that precipitate intra-abdominal actinomycosis include GI surgery, inflammation, and visceral perforation [28,29]. However, in most cases of gastric actinomycosis, it has been impossible to trace the mechanism by which Actinomyces had reached the gastric wall . Our patient had no past history of abdominal surgery or trauma. However, he was on prolonged medication for non-ischemic cardiomyopathy, premature ventricular contractions, renal impairment, hypertension, and dyslipidemia. Such extensive medication may have caused physical or functional gastric mucosal damage that facilitated entry of the organisms into the gastric wall. Numerous drugs, acting through various mechanisms, have been associated with gastric mucosal damage . Age related mucosal atrophy may have also contributed to diminished mucosal resistance.
The rarity of gastric involvement by actinomycosis has been attributed to the high lumenal acidity of the stomach. As a result of the low gastric pH, the organisms may be killed or growth is inhibited .
The usual presenting clinical manifestations of gastric actinomycosis are low-grade fever, epigastric pain, weight loss, and upper GI bleeding [1,3,10,12,20]. One patient developed symptoms of gastric outlet obstruction . The duration of symptoms ranged from two weeks to several years [3,8,9,11,19]. Our patient presented with acute diffuse abdominal pain, abdominal distension, constipation and vomiting for two days duration, with no history of fever. The clinical impression was that of gastric outlet obstruction.
There is no specific radiological or endoscopic appearance for gastric actinomycosis. CT findings have mostly demonstrated an infiltrative lesion with diffuse gastric wall thickening. The appearance suggested adenocarcinoma or lymphoma of the stomach [2,20,32]. In our case, contrast CT-scan showed a significantly distended stomach with thickened wall and abnormal configuration. Similar to radiologic studies, the endoscopic findings of the disease may simulate a gastric neoplasm and include submucosal tumor-like or infiltrative lesions and, occasionally, mucosal ulceration . A non-infectious etiology was initially suspected in our patient based on radiologic and endoscopic findings, possibly adenocarcinoma or lymphoma, and the gastric outlet obstruction subsequently interpreted as functional due to absence of peristaltic movement consequent to infiltration of the gastric wall by actinomycosis. An associated paralytic ileus due to acute pancreatitis may be an alternative explanation for the obstruction as suggested by elevated serum lipase and amylase levels. Such obstruction may have also contributed to the gastric localization of the actinomycosis, so that the clinical manifestations may be a consequence of acute pancreatitis with secondary gastric overinfection by Actinomyces, facilitated by the mucosal damage.
Because of the submucosal localization of the inflammatory process, gastroscopic biopsy specimens usually reveal nonspecific inflammatory changes [3,14,18,19]. In most cases, the diagnosis was made after surgery and histopathological examination of the resected specimen [9,12,19,20,22]. Only two cases have been reported in which the diagnosis of gastric actinomycosis was made on microscopic evaluation of a gastroscopic biopsy specimen [6,8]. In our case, the diagnosis was, likewise, established through histologic examination of gastroscopic biopsies in which abundant PAS, Grocott’s, and Gram positive rod-like and filamentous bacteria, morphologically consistent with Actinomyces were identified. The presence of a brownish, iron negative pigment in the fibrinopurulent inflammatory exudate (that was also visible endoscopically) alerted us to the possibility of actinomycosis which was established by appropriate special staining that revealed the microorganisms. It is well known that the main sources of natural pigments are plants and microorganisms, including Actinomycets .
Culturing is negative in most cases of gastric actinomycosis (>76%) [19,24,25]. In our case, culturing yielded only Streptococcus viridans, another endogenous aerobic/anaerobic facultative commensal present in the oral and GI-tract flora . Despite the negative culture, the typical morphology of the organisms in tissue sections confirmed by positive Grocott, PAS and Gram staining was considered sufficient for the diagnosis of Actinomyces infection with no necessity for culture confirmation.
Most anaerobic bacteria recovered from clinical infections are found mixed with other anaerobic organisms . Polymicrobial infections are known to be more pathogenic for experimental animals than are those involving single organisms . Whether Streptococcus viridans, known to be an organism of low virulence, had contributed to the gastritis in our case remains unclear.
Primary gastric actinomycosis is an indolent infection. If the disease is recognized, the prognosis is good because antibiotic treatment, particularly penecillin is very effective [4,19]. Our patient received 2 doses of IV levofloxacin and 3 doses of IV metronidazole and appeared in a good health status, two weeks after diagnosis.
Althuogh extremely rare, primary gastric actinomycosis should be considered in the differential diagnosis of radiologic and gastroscopic diffuse gastric wall thickening and submucosal tumor-like or infiltrative lesions, particularly in patients with history of abdominal surgery or trauma or those receiving extensive medication. A high level of suspicion is required by the pathologist to achieve diagnosis in gastroscopic biopsies. Subtle changes such as the presence of a pigmented inflammatory exudate should alert the pathologist to perform appropriate special stains to reveal the causative organism.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
The authors acknowledge Dr Amani Al Nemer, Assistant Professor, Microbiology Department, University of Dammam for reviewing the results of H & E and special staining of micro-organisms in tissue sections. The authors also acknowledge the services of Mr Shakir Ahmed and Mrs Maria Rosario Lazaro from the histopathology laboratory of the University of Dammam, Saudi Arabia for conducting the histology technical work.
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