scholarly journals Histopathological study of canine hepatoid gland tumours

Author(s):  
Sudheesh S. Nair ◽  
Sudheesh S. Nair ◽  
Sudheesh S. Nair ◽  
Sudheesh S. Nair ◽  
Sudheesh S. Nair

Hepatoid gland neoplasms arise due to disorganized and uncontrolled proliferation of cells of hepatoid glands. These are the modified sebaceous glands located mainly in the perianal area. Gross and histological findings of canine hepatoid gland tumours were evaluated. Dogs of different breed, age and sex that were presented to Department of Veterinary Surgery and Radiology, College of Veterinary and Animal Sciences, Mannuthy formed the materials for the present study. Grossly, tumours were solitary or multiple irregular shaped intradermal masses. The excisional biopsy samples were collected in 10 per cent neutral buffered formalin after surgical removal of tumour mass. Histopathologically, the masses were encircled by fibrovascular capsule which extended to the parenchyma as tumour stroma, which separated it into lobules. Two cases of hepatoid gland adenoma one case of hepatoid gland epithelioma and two cases of carcinoma were recognised on histopathological examination. Hepatoid adenoma were characterised by proliferation of hepatocyte like hepatoid gland epithelial cells with extensive sebaceous differentiation and were arranged in cords and anastomosing trabeculae. In hepatoid gland epithelioma, many of the cells were basaloid reserve cells with fewer hepatocyte like cells. Histopathological examination of carcinoma revealed irregular arrangement of the hepatoid cells which showed varying degrees of maturation and marked nuclear pleomorphism. The malignant hepatoid cells had abundant eosinophilic cytoplasm and large nuclei with several prominent nucleoli and mitotic figures.

2020 ◽  
Vol 65 (No. 2) ◽  
pp. 84-88
Author(s):  
J Kim ◽  
HJ Kim

A two-year-old spayed female American shorthair cat presented with a rough, circular, exophytic mass on the genital area. The clinical findings and histopathological examination revealed that the mass contained neoplastic mast cells and, thus, was diagnosed as a mast cell tumour. The anatomical location of the mass was not easily accessible for surgical intervention. We administered a targeted therapy using oral imatinib mesylate for eight weeks to reduce the size of the lesion and to facilitate the successful surgical removal. The tumour mass eventually reduced by 21% and was surgically excised. This is possibly the first study to use imatinib mesylate as a tumour reduction neoadjuvant to therapeutically address a feline cutaneous mast cell tumour located in a surgically inaccessible part of the body.


2019 ◽  
Vol 81 (01) ◽  
pp. 071-074
Author(s):  
Jakob Nemir ◽  
Martina Štenger ◽  
Antonia Jakovčević ◽  
Ivan Domazet ◽  
Niko Njirić ◽  
...  

AbstractEctopic adrenal cortical neoplasms of the spinal cord are extremely rare. To date only 10 such cases have been described. We present a case of a 46-year-old woman with lower back pain radiating to the right gluteal and posterior femoral regions, without a history of traumatic injury. Magnetic resonance imaging (MRI) of the thoracic and lumbar spine showed an intradural, extramedullary, well-circumscribed, contrast-enhancing lesion located in the T12–L1 region, hypo- to isointense on T2-weighted imaging, and isointense on T1. Complete surgical removal of the lesion, measuring 3 × 2.5 × 1 cm, was performed. The histopathologic findings revealed the lesion was an ectopic adrenal cortical adenoma, with sheets and nests of round and polygonal cells, mostly round regular nuclei, abundant eosinophilic cytoplasm, 1 mitosis per 10 high-power fields, and without necrosis. These tumors have nonspecific MRI features and therefore can be easily confused with other common spinal tumor types such as ependymoma, schwannoma, meningioma, and metastasis. Although rare, ectopic adrenal spinal cord adenomas should be taken into account in the differential diagnosis of spinal canal intradural neoplasms.


2020 ◽  
Vol 48 ◽  
Author(s):  
Valesca Ferreira Machado de Souza ◽  
Zayan Silva Pereira ◽  
Ianei De Oliveira Carneiro ◽  
Deusdete Conceição Gomes Júnior ◽  
Maria Talita Soares Frade ◽  
...  

Background: Trichoblastoma is a rare skin neoplasm derived from the primitive hair follicle, having epithelial and mesenchymal components. Despite being commonly described as a benign tumor, there are reports in the literature of tumors with characteristics of malignant neoplasia. It affects adult dogs and cats, with no predilection for sex. Although rare, in studies in Brazil the pathology shows variable rates of occurrence. This work describes a case of tricoblastoma in a 4-year-old mixed breed dog, submitted to care at the Veterinary Hospital of the Federal University of Western Bahia (HVU-UFOB).Case: A 4-year-old male mixed breed dog with 7 kg of body weight, was referred to the HVU-UFOB. The main complaint reported by the canine’s tutor was an increase in volume in the region of the animal's face, which evolved slowly, associated with itching, bleeding and sensitivity to touch. During the physical examination, a round, elevated mass was observed in the subcutaneous tissue of the left face, in the mandible region, with local alopecia. On palpation, the neoformation showed a firm consistency, well-defined and fluctuating, with no solutions for continuity or discomfort to touch. The animal's physiological parameters were within the normal for the species. CBC, chest X-rays, abdominal ultrasound and aspiration cytology of the mass were requested. The blood count and image tests did not reveal any changes. On cytological examination, small, grouped basal epithelial cells were observed, characterized by a high nucleus-cytoplasm ratio, monomorphic nuclei and intensely basophilic and pigmented cytoplasm, a suggestive diagnosis of basal cell tumor. Due to the findings, an excisional biopsy of the mass was performed, with margins of 2 cm. The mass with its margins was sent for histopathological examination at the Animal Pathology Laboratory of the HVU. Macroscopically, an expansive mass was observed, covered by skin, was well defined, not encapsulated, distending the dermis, with a dome shape, measuring 8.0 x 5.0 x 4.0 cm in length, white and firm to the cut, with discrete lobulation. Microscopically, there was a proliferation of small cuboidal to elongated cells with a round to oval nucleus of loose chromatin and little evident nucleolus, and of a pale, scarce eosinophilic cytoplasm. Neoplastic cells were sometimes arranged in strings, palisades (ribbon type) or islands and were sometimes seen centrally aggregated emitting strands of cells (medusoid type) separated by moderate fibrovascular stroma, compatible with trichoblastoma. Tissue healing occurred satisfactorily, and the stitches were removed 10 days after the surgical procedure.Discussion: The clinical analysis of the case associated with the cytological and histopathological examination of the lesion allowed the visualization of physical and cellular changes, confirming the diagnosis of trichoblastoma. The animal involved was 4-years-old, within the chronological variability most affected by the tumor. The macroscopic lesions and the location of the neoplasia were also similar to those described in the literature. However, their race (mixed breed) was different from the most evident. Treatment based on total surgical excision of the neoplasia proved to be effective. This work is the first reported in the Western of Bahia describing a case of trichoblastoma in a dog.


Author(s):  
Swetha Gutha ◽  
Shalini Sampath

<p class="abstract">Cutaneous leiomyomas are benign tumors that can be exquisitely painful. Comprise three distinct types such as piloleimyoma, angioleiomyoma, and genital leiomyoma. Piloleiomyomas, derived from arrector pili muscle, are solitary or multiple firm papulonodules located mostly on the extremities and trunk; genital leiomyomas, derived from dartoic, vulvar, or mammary smooth muscle, are solitary or papulonodules located on the scrotum, vulva, or nipple; and angioleiomyomas, include solid, cavernous, or venous subtypes, are derived from the tunica media of small arteries and veins and typically present on the extremities. Excisional biopsy is required for diagnosing all cutaneous leiomyomas Histology shows interlacing fibers of spindle cells with moderate amounts of eosinophilic cytoplasm and a blunt-ended, elongated nucleus with perinuclear halos. Surgical excision is curative for cutaneous leiomyomas, with other management options including medical or destructive therapy. A 36-year-old male patient presented with a 13 years history of painful, multiple lesions over the back. Based on the histopathological examination, imaging, and past medical records, a diagnosis of familial leiomyoma was made. His brother had similar disease. The patient was started on tab gabapentin 300mg at night. Patient advised for carbon dioxide laser excision. The present case report has been reported for its interesting clinical presentations and rarity.</p>


2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Fatemeh Namazi ◽  
Neda Ranjbar Kohan ◽  
Mina Afsar ◽  
Amir Allahdin ◽  
Saeed Nazifi

In the present study, a case of gingival squamous cell carcinoma is described in a 9-yearold sheepdog with a swelling of the left mandible. Plain radiographs of the head revealed a soft tissue mass behind the ventral border of the left mandible. At necropsy, the tumor presented as reddish-brown ulcerated and irregular tumoral masses of the gingiva. In the cytology smear, there were oval to angularshaped squamous epithelial cells with varying immaturity and variable staining and nuclear to cytoplasmic ratios (N:C). Some of the cells showed dyskeratosis. Histopathologically, the tissue sections were composed of the cords and islands of squamous epithelial cells with an abundant eosinophilic cytoplasm, large and ovoid nuclei with a prominent nucleolus. The mitotic figures were moderate. Based on the histopathological findings, the tumor was diagnosed as a moderately differentiated gingival squamous cell carcinoma.


2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Harun Kütahya ◽  
Ali Güleç ◽  
Yunus Güzel ◽  
Burkay Kacira ◽  
Serdar Toker

Schwannomas are also known as neurolemmas that are usually originated from Schwann cells located in the peripheric nerve sheaths. They are the most common tumours of the hand (0.8–2%). They usually present solitary swelling along the course of the nerve however multiple lesions may be present in cases of NF type 1, familial neurofibromatosis, and sporadic schwannomatosis. Schwannomas are generally represented as an asymptomatic mass; however pain, numbness and fatigue may take place with the increasing size of the tumour. EMG (electromyelography), MRI (magnetic resonance imagination), and USG (ultrasound) are helpful in the diagnosis. Surgical removal is usually curative. In this paper, we present a 24-year-old male referred to our clinic for a lump located at the volar side of the left wrist and a lump located in his left palm and numbness at his 3rd and 4th fingers. Total excision was performed for both lesions. Histopathological examination of the masses revealed typical features of schwannoma. At the 6th-month followup the patient was symptom-free except for slight paresthesia of the 3rd and the 4th fingers. For our knowledge, this is the second case in the literature presenting wrist and palm involvement of the median nerve schwannoma.


2016 ◽  
Vol 144 (9-10) ◽  
pp. 535-540
Author(s):  
Aguida Henriques ◽  
Manuela Vidal ◽  
Clarissa Gurgel ◽  
Sanyra Rocha ◽  
Braulio Carneiro ◽  
...  

Introduction. Epithelioid hemangioma is an uncommon benign vasoproliferative neoplasm that usually manifests as multiple red nodules in middle-aged adults. Case Outline. A 52-year-old male patient presented with a one-year history of a nodular lesion in the left buccal mucosa measuring 3 cm. The clinical hypothesis was lipoma. An excisional biopsy revealed a circumscribed lesion composed of lobules of vessels with perceptible or poor lumina, associated with a prominent inflammatory infiltrate consisting of eosinophils, histiocytes and chronic inflammatory cells. The endothelial cells composing the lesion had an epithelioid morphology and contained abundant eosinophilic cytoplasm. Immunohistochemistry for CD34, factor VIII, collagen IV, alpha-smooth muscle actin, and mast cells, as well as histochemical staining with Weigert?s orcein were performed. Conclusion. Vascular proliferations of soft tissues are a diverse and morphologically complex group of lesions that are difficult to diagnose. This report presents a case of oral epithelioid hemangioma, highlighting relevant morphological and immunohistochemical features that could help distinguish this condition from other neoplasms.


2016 ◽  
Vol 66 (4) ◽  
pp. 556-561
Author(s):  
Eun-Joo Lee ◽  
Kim Ah-Young ◽  
Lee Eun-Mi ◽  
Park Jin-Kyu ◽  
Jeong Kyu-Shik

Abstract Malignant pilomatricoma is malignant follicular tumor with only matrical differentiation. Malignant pilomatricoma is rare in dogs. There is little information about sex, breed and age predisposition. There are a few reports of canine malignant pilomatricoma in middle to old age dogs. However, this neoplasm was resected from 1-year-old intact male miniature poodle. The neoplasm was found in the dorsal part of the neck. The mass was firm and protruded. On gross findings the size of the mass was 3×2×1.5cm. The mass was located in the deep dermis and subcutaneous layer. The mass was composed of several lobules of grey-white chalky material. Microscopically, the mass was composed of several large and small lobules. There were basophilic round to oval basaloid cells at the periphery of the lobules. The basophilic cells showed abrupt keratinization. Numerous ghost cells were observed in the center of the mass. The ghost cells had abundant eosinophilic cytoplasm without a nucleus. The basophilic basaloid cells showed numerous atypical mitotic figures. Cellularity was high and pleomorphism was remarkable. No lymphatic metastasis was observed. We reported a rare case of malignant pilomatricoma in a 1-year-old young dog.


2021 ◽  
Vol 19 (2) ◽  
pp. 189-192
Author(s):  
Tolga Düzenli ◽  
◽  
Hüseyin Köseoğlu ◽  
Behice Hande Erenler ◽  
◽  
...  

Introduction. Gastrointestinal stromal tumors (GIST) are tumors of mesenchymal origin which originate from the walls of gastrointestinal system (GIS) organs. Aim. In this case report we aim to discuss the clinical, labaratory and radiological presentation of distal duodenal GIST as a rare and overlooked cause of life-threatining GIS bleeding. Description of the case. A 76-year-old male patient was presented to the emergency department with massive gastrointestinal bleeding. Computerized tomography revealed a mass soft tissue density of 4x4cm at the level of the 3-4th segment of the duodenum. At the endoscopy, there was a deep ulcer in the proximal part of the 3rd segment of the duodenum with a diameter of 2 cm with a bleeding vessel protruding into the lumen. After endoscopic treatments, biopsies were taken from the edges of the ulcer. Histopathological examination revealed a sheet-like infiltration composed of mildly pleomorphic cells with oval-spindle nuclei and abundant eosinophilic cytoplasm in the duodenal lamina propria, as the patient was diagnosed of GIST. Conclusion. GIST and its clinical, labaratory and radiological presentation should be kept in mind in the approach to massive duodenal GIS bleeding.


2020 ◽  
Vol 23 (1) ◽  
pp. 10-12
Author(s):  
Nelema Jahan ◽  
Md. Mamunur Rahman ◽  
Mohammad Shahidul Alam ◽  
Md Saiful Islam

Background: A breast lump is the most common symptom associated with both benign and malignant breast diseases. Therefore, a distinction of benign from malignant lump is of importance for proper management. Though a definitive diagnosis is possible with imaging for all the lesions, histopathological study is proven essential for confirming the diagnosis. Objective: The objective of this study was to evaluate the role of USG and histopathological findings of different breast lump in diagnosis and their comparison. Methods: A prospective study was conducted over a period of one year from January 2017 to December 2017. A total of 116 patients were included in this study. All breast lumps underwent surgery and the ultrasound findings of these lumps were compared with the histopathological findings. Data were collected from these patients by a preformed questionnaire and finally the data were analyzed. Results: Out of 116 patients only 21 cases were reported as malignant in ultrasound report but histopathology revealed 31 malignant patients. On histopathological examination 10 benign cases turned out to be malignant. Conclusion: The present study was undertaken to evaluate in diagnosing breast mass lesions individually by ultrasound and compared with histopathology for definitive management of a patient. Journal of Surgical Sciences (2019) Vol. 23 (1) : 10-12


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