scholarly journals Granulomatous myelitis associated with hemorrhagic syndrome due to consumption of Vicia villosa by cattle

2010 ◽  
Vol 40 (8) ◽  
pp. 1848-1851 ◽  
Author(s):  
Luciana Sonne ◽  
Djeison Lutier Raymundo ◽  
Nadia Aline Bobbi Antoniassi ◽  
Paulo Mota Bandarra ◽  
Paula Rodrigues de Almeida ◽  
...  

An unusual case of spontaneous Vicia villosa poisoning affected a 6-year-old Holstein cow. Although the most striking findings included a generalized hemorrhagic condition associated with granulomatous myelitis, histological lesions typically seen with the vetch-associated systemic granulomatous syndrome were also present. Prominent gross findings were bloody nasal and oral discharges, disseminated hemorrhages, and bloody feces. Generalized hemorrhages associated with infiltration of numerous organs by lymphocytes, plasma cells, macrophages, multinucleated giants cells, and eosinophils were the main microscopic findings. Anti-CD68 immunostaining confirmed the presence of moderate histiocytic infiltrate and multinucleated giant cells in the bone marrow. These changes in the bone marrow probably caused the generalized hemorrhagic changes described here.

2005 ◽  
Vol 42 (6) ◽  
pp. 856-858 ◽  
Author(s):  
E. Oruç

The gross and histopathologic lesions of meningoencephalitis tuberculosa in a 4-year-old Holstein cow showing clinical signs compatible with bovine spongiform encephalopathy are described in this report. Grossly, numerous gray to yellow, firm and caseous nodules were seen on the ventral surfaces of the brain and in the lateral and fourth ventricles. Histopathologically, foci of caseation and dystrophic mineralization were surrounded by multinucleated giant cells, epitheloid macrophages, plasma cells, lymphocytes and fibrous proliferation. Ziehl-Neelsen stains of the lesions revealed masses of slender acid-fast bacilli in the necrotic centers of lesions and within surrounding giant cells.


2001 ◽  
Vol 115 (6) ◽  
pp. 514-516 ◽  
Author(s):  
Andrej Böör ◽  
Ivan Jurkovič ◽  
Imrich Friedmann ◽  
Marian Benický ◽  
Pavol Kočan

The patient was a 54-year-old woman who had been suffering from chronic tubulo-interstitial nephritis for about seven years, requiring haemodialysis. More recently, she developed a polypoid mass in the left nasal cavity causing discomfort on breathing and slight epistaxis. The tumour was of gritty consistency and measured 28 × 8 × 5 mm. Microscopy showed a lobulated almost cystic structure composed of granulation tissue with comparatively few plasma cells and many multinucleated giant cells lining the spaces filled with crystalline deposits of calcium oxalate.


2016 ◽  
Vol 20 (4) ◽  
pp. 349-351
Author(s):  
Daniel Paluzzi ◽  
Tess Peters ◽  
Richard M. Haber

Background: Lipodystrophia centrifugalis abdominalis infantilis (LCAI) is an uncommon dermatological condition characterized by a centrifugally expanding area of lipoatrophy involving the lower abdominal area and is frequently associated with inguinal lymphadenopathy. The average age of onset is 4 years and female individuals from Japan, China, and Korea are affected more often. Objectives: To report the first case of LCAI in a Vietnamese patient. Methods: A complete clinical assessment was done and a biopsy from the affected area was performed. Results: There was an atrophic, slightly hyperpigmented patch at the lower abdomen with prominent underlying vasculature. Inguinal lymphadenopathy was noted on the ipsilateral side. A biopsy showed a lobular panniculitis with fat necrosis and lymphohistiocytic infiltrate with scattered plasma cells and multinucleated giant cells. Conclusion: To our knowledge, this is the first reported case of LCAI in a Vietnamese patient.


2003 ◽  
Vol 6 (2) ◽  
pp. 173-178 ◽  
Author(s):  
Angelica Putnam ◽  
Suzanne Yandow ◽  
Cheryl M. Coffin

Adamantinoma, a rare bone lesion of the tibia and fibula, has two distinct variants, classic adamantinoma and osteofibrous dysplasia-like adamantinoma. Composite lesions have not been described. Aneurysmal bone cyst is a benign cystic lesion which may also occur in the tibia and fibula. We report an unusual case of classic adamantinoma with osteofibrous dysplasia-like areas and foci of secondary aneurysmal bone cyst with prominent giant cells. A lesion was diagnosed in a 17-year-old girl with a 14-year history of a slowly enlarging left tibial mass and increasing deformity. Pathologically, the predominant pattern was classic adamantinoma, with minor foci of osteofibrous dysplasia-like adamantinoma and areas of secondary aneurysmal bone cyst with abundant multinucleated giant cells. We report the clinical, radiologic, and pathologic features of this case, and summarize lesions associated with secondary aneurysmal bone cyst. To our knowledge, the association of adamantinoma with secondary aneurysmal bone cyst has not been previously reported.


Author(s):  
Keval A. Patel ◽  
Kinalee P. Chothani ◽  
Bimal Patel ◽  
Dhaneshwar N. Lanjewar

Xanthogranulomatous inflammation of ovary is a rare disease that is characterized by presence of large number of lipid laden macrophages with an admixture of neutrophils, lymphocytes, plasma cells and multinucleated giant cells. It is misdiagnosed as ovarian tumour that leads to extensive surgery including hysterectomy. In this report we describe a case of Xanthogranulomatous salpingo-oophoritis along with review of literature.


2017 ◽  
Vol 45 (1) ◽  
pp. 7
Author(s):  
Amaro Francisco Viero Silveira ◽  
Welden Panziera ◽  
Susy Hermes de Sousa ◽  
Bianca Santana Cecco ◽  
Claiton Ismael Schwertz ◽  
...  

Background: Hairy vetch (Vicia spp.) is a high-protein source forage to cattle. The poisoning is clinically characterized by a systemic granulomatous disease, which causes dermatitis, diarrhea, decreased milk production and weight loss. The specie of hairy vetch related to systemic granulomatous disease in cattle is Vicia villosa. This work aims to describe the epidemiological, clinical, gross, microscopic and immunohistochemistry features of the skin lesions caused by the consumption of V. villosa in cattle affected by the systemic granulomatous disease.Materials, Methods & Results: A retrospective study of necropsy and biopsy exams performed between the period of 2005-2016 aiming for cattle with systemic granulomatous disease after consumption of hairy vetch was carried out in the archives of the Setor de Patologia Veterinária from the UFRGS. Epidemiological data included the sex, age, and breed of the animals affected. Gross and microscopical lesions, in addition to the immunohistochemistry anti-T lymphocytes (CD3), anti-B lymphocytes (CD79a), and anti-macrophages (CD68) features, were evaluated. The histological lesions and immunohistochemistry staining were quantified in mild (+), moderate (++), and severe (+++). The diagnosis of systemic granulomatous disease with skin lesions after consumption of Vicia villosa was observed in eight cattle. All animals were females, with  5-8 year-old (average 6.6 years), Holstein Friesian cattle (7) and Jersey (1) breeds. These cattle had a clinical history of severe pruritus, anorexia, apathy, decreased milk production, weight loss, and hyperthermia. Grossly, lesions were characterized by alopecia (8/8), crusts (7/8), lichenification and seborrhea (2/8), and exudative lesions (2/8), and involved the head (7/8), limbs (5/8), neck (4/8), trunk (4/8), perineum area (3/8), udder (3/8), and tail (3/8). Histology revealed a mild to moderate inflammatory infiltrate (7/7), composed by lymphocytes (7/7), macrophages (7/7), occasional eosinophils, and rare multinucleated giant cells (1/7). It was also classified in mild to severe perivascular dermatitis (7/7), mild to moderate perifolliculitis (4/7), superficial dermatitis (3/7), moderate to severe mural folliculitis (2/7), and hidradenitis (1/7). Another findings were moderate apocrine sweat gland ectasia, mild to moderate orthokeratotic hyperkeratosis, mild to moderate spongiosis, mild to moderate acanthosis, mild to severe serocellular crusts, mild pigmentary incontinence, mild to severe Munro’s microabscesses, mild to moderate hydropic degeneration, apoptosis, ulcers, mild to moderate superficial edema of the dermis, variable epitheliotropism and erosions.  Immunohistochemistry of all skin sections had mild to severe staining for T cell (CD3), mild staining for macrophages (CD68), and immunostaining was rare (4/7) or absent (3/7) for B cells (CD79a).Discussion: Cutaneous lesions observed in this study were similar to those previously described by other authors for this condition, and were characterized by focal to coalescent areas of alopecia, lichenification and seborrhea, associated clinically to a severe pruritus. Histologically, these consisted of perivascular dermatitis, and perifolliculitis with an inflammatory infiltrate composed predominantly by lymphocytes, macrophages, with occasional eosinophils and multinucleated giant cells. Immunohistochemistry demonstrates a marked immunostaining for T cells, while it was mild for macrophages, which reinforces the involvement of the delayed type hypersensitivity (type IV) reaction in the pathogenesis of the disease.


1992 ◽  
Vol 4 (3) ◽  
pp. 318-325 ◽  
Author(s):  
Roger J. Panciera ◽  
Derek A. Mosier ◽  
Jerry W. Ritchey

Hairy vetch poisoning (vetch-associated disease) of cattle is a generalized disease characterized pathologically by infiltration of skin and many internal organs by monocytes, lymphocytes, plasma cells, and often eosinophils and multinucleated giant cells and clinically by dermatitis, pruritis, often diarrhea, wasting, and high mortality. The disease was experimentally reproduced in an adult Angus female that had recovered from the natural disease 1 year earlier. She developed dermatitis on the 11th day of vetch feeding, and despite withdrawal from the vetch diet on the 12th day, death occurred 24 days after first day of vetch feeding. The cow developed lymphocytosis and hyperproteinemia. The results of other hematologic evaluations, blood chemical profiles, urinalysis, and cutaneous hypersensitivity tests using vetch lectin were normal. Lymphocyte blastogenesis studies with vetch lectin were not interpretable. Necropsy revealed gross lesions characteristic of the disease in the skin, heart, kidney, adrenal, and lymphoid tissues. Microscopically there was typical cellular infiltration in those organs and in the thyroid, liver, pancreas, salivary and mammary glands, urinary bladder, corpus luteum, and cerebral meninges. Cutaneous apocrine gland necrosis was present. The inflammatory reaction has qualities of a type-IV hypersensitivity reaction. Hypersensitivity may occur when constituents of the ingested plant are absorbed and act as antigens that sensitize lymphocytes and evoke the multisystemic granulomatous inflammatory response that characterizes the disease. Alternatively, vetch lectin may directly activate T lymphocytes to initiate the cellular response. Vetch-like diseases have been associated with a variety of diets that did not contain hairy vetch. The gross and histopathologic lesions of the vetch-associated and the vetch-like diseases are not mimicked in quality and distribution by any other disease.


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