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Final Diagnosis:

Heterobilharzia americana

Clinical History:  A 5-year-old intact female Shih-Tzu presented for evaluation of vomiting, diarrhea, and decreased appetite.  She was in heat approximately one month previous to onset of clinical signs.  Radiographs of the abdomen revealed mildly distended bowel loops.  A presumptive clinical diagnosis of pyometra was made and an exploratory laparotomy was performed.

Surgical Findings:  Laparotomy revealed a mildly turbid fluid within the peritoneum.  Multiple firm nodules (approximately 0.5 cm in diameter) were present in the right lobe of the pancreas, small intestinal serosa and enlarged mesenteric lymph nodes.  The uterus was mildly distended by fluid.  Biopsy specimens from the pancreas, lymph node, and jejunum were submitted for histopathology.  An ovariohysterectomy was performed after the biopsies and uterus and ovaries were also submitted for histologic evaluation.

Histologic Findings: The lymph node contained numerous round to oval, approximately 80 µm wide ova with a yellow to tan, thick hyalinized wall distributed primarily in the paracortex.  Many of the ova contained developing miracidium, although a few were empty.  A marked inflammatory reaction surrounded individual ova and consisted of many epithelioid macrophages with fibrosis, eosinophils, neutrophils, lymphocytes, plasma cells, and few multinucleated giant cells.

  The small intestine (jejunum) contained ova and granulomatous inflammation distributed transmurally and near venules, likely arborizing from the mesenteric veins.  Similar ova and granulomatous inflammation was observed in the pancreas.

  Uterus and ovaries were histologically unremarkable.

Ancillary testing:  Fecal sedimentation in saline revealed miracidia-laden eggs.

SmIntestine_4x.jpgSmall intestine with transmural parasitic ova containing miracidium and surrounded by granulomatous inflammation.  Eggs are consistent with Heterobilharzia americana.

 

 

mesentericLN_40x.jpg

Mesenteric lymph node with numerous parasitic ova and surrounded by granulomatous inflammation.  Eggs are consistent with Heterobilharzia americana.

 

 

Hetero_037 copy.jpgMiracidia-laden trematode egg consistent with Heterobilharzia americana from fecal sedimentation.  Note the miracidium within a thick refractile capsule and no operculum.

 

 

Discussion:  Heterobilharzia americana, classified as a schistosome, is a blood fluke of wild and domestic carnivores and is widespread in southern Atlantic and gulf coast states (Florida, Louisiana, Mississippi, Texas, Georgia, North Carolina, South Carolina) as well as east central states and southeast Kansas.  The life cycle of H. americana is indirect, involving an aquatic snail (Lymnaea cubensis and Pseudocuccinea columella) as the intermediate host.  Cercariae that are released from the snail intermediate host infect dogs and wildlife through  direct skin penetration.  Clinically significant H. americana infection includes massive inflammation leading to intestinal disorders, dehydration, pancreatic insufficiency, and systemic dissemination.  Antemortem diagnosis requires fecal sedimentation in 0.9% NaCl to identify characteristic trematode eggs.  Schistosome ova are large (70-90µm), non-operculated, and contain miracidium.  Unfortunately, schistosome larvae were not identified in multiple tissue sections.  Diagnosis was based on fecal sedimentation by the Clinical Parasitology Laboratory at Purdue University as well as histopathologic evaluation of ova.  The dog was presumably infected while vacationing in Florida in July and subsequently became ill in August of the same year.  Treatment with fenbendazole for 14 days was initiated and repeated after three weeks.  One month following administration of high doses of fenbendazole, no ova were detected on sedimentation, feces were formed, and appetite and activity were normal.

-by Dr. Abigail Durkes, ADDL Graduate Student

References:

  1. Flowers J, Hammerberg B et al: 2002. JAVMA 220(2):193-96.

  2. Goff W and Ronald J: 1982. American Journal of Veterinary Research 42:1775-76.

  3. Malek E, Ash L et al: 1961. Journal of Parasitology 47:619-23.

  4. McKown R, Veatch J et al: 1991.  Journal of Wildlife Diseases 27(1): 156


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