LFLeonardo Schuler Faccini

Leonardo Schuler Faccini

*This is an algorithmically generated author record based on publicly available information.

Leonardo Schuler Faccini has a total of 23 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Outbreak of leishmaniasis caused by Leishmania enriettii in guinea pigs (Cavia porcellus)

    by Cibele Ribeiro, Kethleen N. Koubiach, Leonardo S. Faccini, Mariana C. Teixeira, Fábio A. Schüür, Vanete Thomaz-Soccol, Claudio S.L. Barros, Ana Carolina B. Coelho

    We describe an outbreak of leishmaniasis in seven guinea pigs (Cavia porcellus) in which nodular ulcerated skin lesions of varying sizes were observed in the nasal cavity, upper lip, pinnae, vulva, and periarticular region of the limbs. Cytologic exam of collected samples of the lesions in the auricle of one of the animals revealed macrophages containing parasitophorous vacuoles of approximately 4.0μm in diameter in their cytoplasm with morphology suggestive of Leishmania sp. Although skin lesions spontaneously regressed in two of the Guinea pigs, only one survived. All six animals that died were necropsied. Grossly, all animals showed bloody nodular cutaneous lesions with crusts. One of the guinea pigs had distended dark red and firm lungs. Histopathology of the skin lesions revealed histiocytic interstitial acanthotic dermatitis associated with a myriad of Leishmania organisms within macrophages cytoplasm. In the lung, the lesions were characteristic of broncho-interstitial pneumonia with focal infiltrates of neutrophils, epithelioid macrophages, and multinucleated giant cells containing 2µm basophilic amastigotes with morphology compatible with Leishmania spp. A focal granulomatous lesion ,associated with the causal agent in the lung is a novel description of leishmaniasis in guinea pigs caused by L. enriettii. The polymerase chain reaction (PCR) technique with mini-exon primer performed in samples of lesions from two affected guinea pigs was positive and equal to the reference strain, identifying Leishmania enriettii. The cytological, macroscopic, and histological lesions associated with the PCR technique allowed the diagnosis of leishmaniasis and the identification of the specie L. enriettii.


  • Open Access

    Dermatophilosis in ruminants and horses in the southern region of Rio Grande do Sul between 2009-2019

    by Leonardo Schuler Faccini, Fabano Rosa Venancio, Taina dos Santos Alberti, Haide Valeska Scheid, Rosimeri Zamboni, Ana Lucia Schild

    This study has the objective of describing the epidemiology of dermatophilosis in cattle, horse, and sheep in the southern of Rio Grande do Sul during a period of 10 years. Data was gathered of all cases/outbreaks of dermatophilosis in ruminants and equines There were 44 (49,4%) diagnoses of dermatophilosis out of 89 cases presenting non-proliferative cutaneous lesions. Of these, 13 were in cattle, 29 in horses, and two were in sheep. It was made a consultation to the Hospital de Clínicas of Porto Alegre/RS and DATASUS database to determine the occurrence of dermatophilosis in humans due to its zoonotic characteristic. It was observed that both in public hospitals and in the SUS database, dermatopathies are recorded in a non-specific way, and with dermatophilosis being a dermatopathy with nonspecific lesions, the definitive diagnosis with the characterization of the agent is not made. The results of this study allowed to conclude that dermatophilosis has a relative importance in domestic species since mortality not occurs in cattle and horses. Still, one must consider the lower dairy production in cattle. In sheep, there was mortality and losses due to the fall in wool quality, and the disease should be considered in diagnosing skin lesions in this species. In humans, the disease is underreported and the possibility of its occurrence in rural areas is alerted; however, cases rarely reach the laboratory.


  • Open Access

    Craniomandibular Osteopathy in Mixed Breed Dogs

    by Taina dos Santos Alberti, Carolina Buss Brunner, Fabiano da Rosa Venâncio, Thaís Cozza Dos Santos, Leonardo Schuler Faccini, Jéssica Line Farias, Josiane Bonel

    Background: Craniomandibular osteopathy (CMO) is a degenerative, osteopetrotic, and self-limiting bone disease that is rare in the canine species. The most affected bones and joints are the branches of the mandible, tympanic bulla, and temporomandibular joint (TMJ) with generalized thickening of the bone trabeculae, increased lines of bone cementation, and bone proliferation. The aim of the present study was to evaluate 2 cases of CMO in mixed-breed dogs belonging to the same litter sent to the Laboratório Regional de Diagnóstico, Faculdade de Veterinária, Universidade Federal de Pelotas (LRD / FV / UFPel). Cases: Three canines (mixed-breed, 2 female and 1 male) belonging to the same litter presented at eight months of age with increases in volume and pain in the face, difficulties in moving the jaw, anorexia, and sialorrhea. The 2 female dogs were euthanized and sent to LRD / FV / UFPel for necropsy. The animals underwent radiography of the left and right lateral and dorsoventral lateral projections in the imaging sector of the Hospital de Clínicas Veterinária (HCV) at UFPel. During the necropsy, fragments of organs from the abdominal and thoracic cavities, as well as the central nervous system and head bones, were collected and fixed in 10% buffered formalin. The tissue samples were cleaved, processed routinely, embedded in paraffin, cut into sections of 3 µm thickness, and stained using hematoxylin and eosin (HE). The bone fragments were decalcified in a 50/50 solution of 8% hydrochloric acid and 8% formic acid and subsequently cleaved and stained with HE. The head and jaw of one of the animals was dissected and subjected to maceration in water at room temperature. Radiographic examination of the two remaining animals showed irregular and exuberant bone proliferation in the mandible and temporomandibular region. In the tympanic bullae, occipital bone, and zygomatic process, thickening of the structures was observed with increased opacity. On necropsy, the animals were cachectic with marked muscle atrophy and increased volume of the mandibular branches and head bones, in addition to marked edema in the adjacent subcutaneous tissue. The regional lymph nodes were enlarged, and in one of the animals, bilateral lesions in the femurs were also observed. In the head subjected to biological maceration, areas of bone proliferation and rarefaction were observed, with increased volume and destruction of the TMJ. On histopathological evaluation of the ventral portion of the mandibular bodies, a network of bony trabeculae was observed, composed of a chondroid matrix with different degrees of mineralization. The cortical portion of the bones exhibited loss of lamellar compactness, with greater spread of the bone trabeculae. The bone trabeculae were perpendicular to the long axis of the cortical of the mandible and were distributed in the medullary spaces, presenting some dense foci of inflammatory infiltrates composed predominantly of neutrophils, lymphocytes, and plasma cells. Discussion: The breeds most predisposed to developing CMO are the West Highland White Terrier and Scottish Terrier; however, the disease has also been described in other non-Terriers. Nevertheless, there are no descriptions in the literature of mixed-breed animals (SRD), with this report being the first of CMO in SRD dogs. The bones most frequently affected in CMO are those of the head. In Terrier dogs, the TMJ is also affected. In the cases of this study, severe CMO occurred, affecting both the head bones and TMJ, and in 1 of the animals, it also affected the femurs. Although CMO has not previously been reported in SRD dogs, the condition can seriously affect these animals, and differential diagnosis should always be made. Keywords: degenerative bone disease, bone proliferation, lion jaw, TMJ. Título: Osteopatia craniomandibular em cães sem raça definida Descritores: doença óssea degenerativa, proliferação óssea, mandíbula de leão, ATM.


  • Open Access

    Aprosopia/holoprosencephaly in a stillborn puppy: when the face predicts the brain

    by Clairton Marcolongo Pereira, Tayná B. Silva, Laiz Zaché Roque, Bárbara Barros, Luiz Alexandre Moscon, Ana Lucia Schild, Claudio S. L. Barros, Leonardo Schüler-Faccini, Lavinia Schuler-Faccini

    In a litter of three puppies, one was stillborn and had facial and brain defects. Fusion of the maxilla and mandible and absence of the face were observed. The forebrain (telencephalon and the diencephalon) was reduced in size and fused, and the telencephalic longitudinal fissure, olfactory bulbs, and optic nerves were absent (Figures 6 and 7). Lissencephaly was observed in the telencephalon and cerebellum. A diagnosis of aprosopia/holoprosencephaly was made.