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Read-Only Case Details Reviewed: Apr 2008

JPC SYSTEMIC PATHOLOGY

NERVOUS SYSTEM

February 2023

N-P12

 

Slide A: Signalment (JPC #1652892): Military working dog

 

HISTORY: This dog developed convulsions and ataxia.

 

HISTOPATHOLOGIC DESCRIPTION: Cerebrum, meninges: Focally elevating and expanding the meninges and compressing the adjacent gray and white matter is a larval cestode with a 2mm diameter invaginated scolex and a large, 4mm diameter bladder (cysticercus) surrounded by a connective tissue capsule. The capsule is composed of multiple layers of fibroblasts and collagen with rare lymphocytes, and blends with the meninges. The bladder wall is characterized by an up to 20 µm eosinophilic tegument surrounding spongy parenchyma with many embedded, oval, 10 x 30 µm, basophilic to clear, calcareous corpuscles. Multiple sections of sucker are visible within the scolex.  In the adjacent compressed gray matter and focally extending into the white matter, there is mild vacuolation (spongiosis) and dissolution of the neuropil (compression atrophy); few neurons with hypereosinophilic, shrunken, angular cytoplasm and pyknotic nuclei (neuronal necrosis); few reactive astrocytes with abundant eosinophilic cytoplasm (gemistocytes); and few swollen, degenerate axons within dilated myelin sheaths (spheroids).

 

MORPHOLOGIC DIAGNOSIS: Cerebrum, meninges: Cysticercus, focal, with gray and white matter spongiosis, neuronal necrosis, and gemistocytosis, breed not specified, canine.

 

ETIOLOGIC DIAGNOSIS: Cerebral cysticercosis

 

ETIOLOGY: Cysticercus cellulosae (larval stage of Taenia solium)

 

CONDITION: Cysticercosis

 

Slide B: Signalment (JPC #2026219): 2-year-old Corriedale ram

 

HISTORY: This ram was circling, with a head tilt, had a peculiar high-stepping gait, was grinding its teeth, and had an aversion to flocking behavior. He was one of several similarly affected sheep examined in Peru.

 

HISTOPATHOLOGIC DESCRIPTION: Brainstem: Multifocally elevating and expanding the meninges and minimally compressing the subjacent neuroparenchyma are few variably sized connective tissue capsules that each surround a single fluid-filled bladder that contains multiple larval cestodes (coenurus) characterized by up to 700 µm diameter invaginated scolices that often contain one or two suckers and a rostellum with refractile, chitinized hooks. The bladder wall is characterized by an up to 400 µm thick eosinophilic tegument surrounding spongy parenchyma with many embedded, oval, 10 x 30 µm, basophilic to clear, calcareous corpuscles. The meninges and connective capsules are infiltrated by numerous nodular aggregates and scattered inflammatory cells composed of varying numbers of neutrophils, lymphocytes, plasma cells, eosinophils, macrophages, multinucleate giant cells (foreign body and Langhans type), abundant eosinophilic cellular and karyorrhectic debris (necrosis), and many congested blood vessels. There are multifocal regions within the meninges that have loss of differential staining and retention of architecture (coagulative necrosis). Multifocally within the meninges, there are granulomas up to 700µm in diameter characterized by a central zone of necrosis surrounded by a concentric rim of epithelioid macrophages, bounded by a layer of numerous lymphocytes, plasma cells, and scattered eosinophils, which is further bounded by few fibroblasts on a thin collagenous matrix, and few multinucleate giant cells. Focally, a nerve rootlet is minimally infiltrated by few lymphocytes and plasma cells. Scattered macrophages and multinucleate giant cells frequently contain an intracytoplasmic brown globular pigment (hemosiderin). Multifocally, in areas of compressed white matter, lymphocytes and plasma cells expand Virchow-Robin space (perivascular cuffing) and affected blood vessels have hypertrophic endothelium (reactive). Multifocally, there is mild vacuolation of the parenchyma (spongiosis), and gliosis.

 

MORPHOLOGIC DIAGNOSIS: Brainstem: Meningitis, granulomatous and lymphoplasmacytic, diffuse, severe, with spongiosis, gliosis, perivascular cuffing, and multiple meningeal coenuri, Corriedale, ovine.

 

CAUSE: Coenurus cerebralis (larval stage of Taenia multiceps)

 

ETIOLOGIC DIAGNOSIS: Meningeal coenurosis

 

CONDITION: "Gid" or "Sturdy"

 

GENERAL DISCUSSION:

 

PATHOGENESIS:

Cysticercus cellulosae/Taenia solium:

  • Cysticerci encyst within striated muscle > avoidance of immune-mediated destruction by inactivating elements of the complement system > release enzymes that cause lysis to allow room for the growing connective tissue capsule

Coenurus cerebralis/Taenia multiceps:

  • The pathology is twofold: (1) larval migration causes necrosis and inflammation within the CNS > (2) capsule expansion compresses neural tissue, and may even perforate the overlying skull > can lead to increased intracranial pressure, hydrocephalus, and necrosis of the adjacent brain

 

LIFE CYCLE:

Cysticercus cellulosae/Taenia solium:

Coenurus cerebralis/Taenia multiceps:

  • Similar to above, but the dog (definitive host) carries the adult tapeworm, and coenuri develop within the CNS of sheep (intermediate host)

 

TYPICAL CLINICAL FINDINGS:

Cysticercus cellulosae/Taenia solium:

Coenurus cerebralis/Taenia multiceps:

  • Neurological signs in sheep (blindness, incoordination, circling, head pressing), paresis or paralysis

 

TYPICAL GROSS FINDINGS:

Cysticercus cellulosae/Taenia solium:

  • Multiple small translucent vesicles filled with clear fluid in striated muscle (heart, masseter, tongue and shoulder muscles) and occasionally meninges and brain

Coenurus cerebralis/ Taenia multiceps:

 

TYPICAL LIGHT MICROSCOPIC FINDINGS:

Cysticercus cellulosae/Taenia solium:

Coenurus cerebralis/Taenia multiceps:

 

DIFFERENTIAL DIAGNOSIS:

Cestode larvae in the CNS of cattle/small ruminants:

 

COMPARATIVE PATHOLOGY:

 

 

 

ADULT

TAPEWORM

DEFINITIVE HOST

LARVAL (METACESTODE) FORM

INTERMEDIATE HOST

SITE - IH

Taenia saginata

man

Cysticercus bovis (M-P03)

cattle

muscle

Taenia solium

man

Cysticercus cellulosae

pig, NHPs, man

Muscle, meninges, brain

Taenia  multiceps

dog

Coenurus cerebralis

sheep, cattle, goats, horses, man

CNS

Taenia hydatigena

dog

Cysticercus tenuicollis

sheep, cattle, pig

peritoneum

Taenia ovis

dog

Cysticercus ovis

sheep, goats

muscle

Taenia pisiformis

dog

Cysticercus pisiformis

rabbits, hares

peritoneum

Taenia serialis

dog, fox

Coenurus serialis

rabbit

subcutaneous and intermuscular connective tissue

Taenia taeniaeformis

cat

Cysticercus fasciolaris (strobilocercus) (D-P22)

mouse, rat, hamster

liver

Taenia krabbei

wild carnivores in temperate and arctic climates

Cysticercus tarandi

reindeer, gazelle, moose, other wild ruminants

muscle

Versteria sp. (including Taenia mustelae (J Vet Diagn Invest, 2022)

weasels

 

rodents, man, NHPs

many organs (most severe in lungs, liver, brain)

Taenia crassiceps

canid

Cysticercus longicollis

lemurs

peritoneum, subcutis, thoracic cavity

Diphyllobothrium spp.

bear, man, cats, swine, piscivorous mammals

sparganum

copepod, fish

muscle

Diphyllobothrium pacificum

seal, sea lion

sparganum

marine birds

muscle

Spirometra sp

dogs, cats, lynx, racoons

Plerocercoid

“sparganum”

Amphibians, reptiles, man, NHPs, rodents

body cavity, muscle, or subcutaneous tissues

Mesocestoides spp.

dogs, birds, other mammals

tetrathyridia

Insect/mite and vertebrate (mammals, NHPs,reptiles, birds) 

body cavities, liver, lungs

Raillietina sp., Choanotenia sp., Davainea sp., Hymenolepis sp., Amoebotaenia sp.

birds

 

many invertebrates

 

Hymenolepis diminuta, Rodentolepis microstoma, Rodentolepis nana (the dwarf tapeworm)

rodents

 

arthropods, man

lamina propria of small intestine (R. nana),

Cittotaenia variabilis

domestic rabbits

 

orbatid mites

 

 

 

REFERENCES:

  1. Barthold SW, Griffey SM, Percy DH. Pathology of Laboratory Rodents and Rabbits. 4th ed. Ames, IA: John Wiley & Sons; 2016: 85,153,190,302.
  2. Boulianne M, Brash ML, Charlton BR, et al., edgs. Avian Disease Manual. 7th ed. Jacksonville, FL: American Association of Avian Pathologists, Inc.; 2013: 158, 178.
  3. Bowman DD. Georgi's Parasitology for Veterinarians. 10th ed. St. Louis, MO: Elsevier Saunders; 2014:143-150; 413-417.
  4. Cantile C, Youssef S. Nervous system. In: Maxie MG, ed. Jubb, Kennedy, and Palmer’s Pathology of Domestic Animals. Vol 1. 6th ed. St. Louis, MO: Elsevier; 2016: 389.
  5. Cooper BJ, Valentine BA. Muscle and tendon. In: Maxie MG, ed. Jubb, Kennedy, and Palmer’s Pathology of Domestic Animals. Vol 1. 6th ed. St. Louis, MO: Elsevier; 2016:239-240.
  6. Crouch EEV, Hollinger C, Zec S, and McAloose D. Fatal Hymenolepis nana cestodiasis in a ring-tailed lemur (Lemur catta). Vet Pathol. 2022; 59(1): 169-172. 
  7. Gardiner CH, Poynton SL. An Atlas of Metazoan Parasites in Animal Tissues. Washington, DC: Armed Forces Institute of Pathology; 1999:50-53.
  8. Lowenstine LJ, McManamon R, Terio KA. Apes. In: Terio KA et al, eds. Pathology of Wildlife and Zoo Animals. San Diego, CA: Elsevier; 2018: 400.
  9. Matz-Rensing K, Lowenstine LJ. New World and Old World monkeys. In: Terio KA et al, eds. Pathology of Wildlife and Zoo Animals. San Diego, CA: Elsevier; 2018: 365-366.
  10. McAloose D, Stalis IH. Prosimians. In: Terio KA et al, eds. Pathology of Wildlife and Zoo Animals. San Diego, CA: Elsevier; 2018: 337-338.
  11. Miller AD, Porter BF. Nervous system. In: Zachary JF, ed. Pathologic Basis of Veterinary Disease. 7th ed. St. Louis, MO: Elsevier; 2022: 931.
  12. Niedringhaus KD, Ganoe LS, Lovallo M, et al. Fatal infection with Versteria sp. In a muskrat, with implications for human health. J Vet Diagn Invest. 2022; 34(2):314-318.
  13. Straight K, Else JG, Eberhard ML. Parasitic Diseases of Nonhuman Primates. In: Abee CR, et al, eds. Nonhuman Primates in Biomedical Research. Vol 2. 2nd ed. San Diego, CA: Elsevier; 2012: 255-258.
  14. Uzal FA, Plattner BL, Hostetter JM. Alimentary system. In: Maxie MG, ed. Jubb, Kennedy, and Palmer’s Pathology of Domestic Animals. Vol 2. 6th ed. St. Louis, MO: Elsevier; 2016:221-224, 255.
  15. Valentine BA. Skeletal Muscle. In: Zachary JF, ed. Pathologic Basis of Veterinary Disease. 7th ed. St. Louis, MO: Elsevier; 2022: 1007.e1.

 

 

 

 


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