scholarly journals Invasive nasal histiocytic sarcoma as a cause of temporal lobe epilepsy in a cat

2018 ◽  
Vol 4 (2) ◽  
pp. 205511691881117 ◽  
Author(s):  
Koen M Santifort ◽  
Ben Jurgens ◽  
Guy CM Grinwis ◽  
Ingrid Gielen ◽  
Björn P Meij ◽  
...  

Case summary A 10-year-old neutered female domestic shorthair cat was presented with an acute onset of neurological signs suggestive of a right-sided forebrain lesion, temporal lobe epilepsy and generalised seizure activity. MRI of the head revealed an expansile soft tissue mass in the caudal nasal passages (both sides but predominantly right-sided) involving the ethmoid bone and extending through the cribriform plate into the cranial vault affecting predominantly the right frontal lobe and temporal lobe. Histopathological examination of the tumour revealed a histiocytic sarcoma. Relevance and novel information This is the first report of a cat with clinical signs of temporal lobe epilepsy due to an invasive, histiocytic sarcoma. Histiocytic sarcoma, although rare, should be included in the list of differential diagnoses for soft tissue masses extending through the cribriform plate. Other differential diagnoses are primary nasal neoplasia (eg, adenocarcinoma, squamous cell carcinoma, chondrosarcoma and other types of sarcomas), lymphoma and olfactory neuroblastoma. Temporal lobe epilepsy in cats can be the consequence of primary pathology of temporal lobe structures, or it can be a consequence of pathology with an effect on these structures (eg, mass effect or disruption of interconnecting neuronal pathways).

2021 ◽  
Vol 49 ◽  
Author(s):  
Millena Oliveira Firmino ◽  
Ismael Lira Borges ◽  
Gian Libânio Da Silveira ◽  
Mikael Leandro Duarte De Lima Tolentino ◽  
Erika de Lourdes Gomes Queiroz ◽  
...  

Background: Lymphomas are considered uncommon in goats, being the multicentric form with the highest number of cases for the species. Primary intranasal lymphomas are often diagnosed in dogs, cats, and humans. In the literature, there is only a description of a multicentric case involving the frontal sinuses and mucosa of the nasal cavity in a goat; therefore, it is important to describe unusual cases of this disease for the inclusion of new clinical and pathological characteristics in the ruminant clinic medicine. The objective of this work is to describe a case of T-cell lymphoma in the nasal cavity of a young goat.Case: The animal had dyspnea and respiratory noise for 15 days. Clinical examination showed nodulation in the right nasal cavity associated with serosanguinous secretion. Tracheostomy was performed; however, after 30 days the animal was euthanized. A sagittal plane of the head showed a pinkish-gray mass in the right and left nasal cavity, with a smooth, multilobulated surface, smooth adhering to the rostral portion of the dorsal concha and occluding the dorsal nasal meatus. Submandibular lymph nodes were slightly enlarged. Histopathological examination of the nasal cavity revealed a non-encapsulated, poorly delimited and ulcerated tumor composed of round cells arranged in a mantle supported by a discrete fibrovascular stroma extending the mucosa and lamina propria. Cells were round with sparse, eosinophilic and poorly delimited cytoplasm. Nuclei varied from round to elongated with condensed chromatin and evident nucleoli. Occasionally, aberrant nuclei, reniform shape and multinucleated cells were seen. Pleomorphism was moderate characterized by anisocytosis and anisocariosis. Typical and atypical mitosis were frequent (0-4 per field of highest magnification [400x]). Amidst the neoplasm, there were multifocal areas of necrosis and hemorrhage associated with a mild lymphocytic inflammatory infiltrate. Immunohistochemistry showed positive immunostaining for Vimentin antibodies and CD3, and negative for pan CK and CD20.Discussion: The lymphomas immunophenotyping is little used when it comes to farm animals, and there are few studies that use this technique for the definitive diagnosis of these neoplasms for small ruminants. The use of this technique must be considered in each case, in order to determine the pathogenesis, the accurate diagnosis and the origin of the neoplastic lymphocytes. In goats, T-cell lymphomas are the most diagnosed, although cases of multicentric B-cell lymphomas with ocular involvement have been diagnosed. In view of the clinical picture of the case described, infectious rhinitis already described in goats, such as aspergillosis and protothecosis, should be included as differential diagnoses. However, the anatomopathological findings facilitate the direction of the diagnosis, since infectious rhinitis presents as nodules / ulcerated masses or focal areas of necrosis associated with purulent secretion and in the histopathological examination it is possible to observe the intralesional etiological agents. In addition, the enzootic ethmoidal tumor must be included, as it has similar clinical signs and affects young animals, but they are adenomas/adenocarcinomas that affect the ethmoidal nasal shells induced by a retrovirus. Lymphomas in the caprine species are rare in the Northeastern semi-arid, but that in the present diagnostic routine occasionally occurs, being important the first description of its nasal shape for its inclusion in the differential diagnoses of diseases that present with clinical obstruction and dyspnea for the species. Keywords: hematopoietic neoplasia, immunophenotyping, lymphocytes, dyspnea.Descritores: neoplasia hematopoietica, imunofenotipagem, linfócitos, dispneia.Título: Linfoma de células T na cavidade nasal de caprino. 


2019 ◽  
Vol 6 (3) ◽  
pp. 996
Author(s):  
Mayank Bhasin ◽  
Karamjot Singh Bedi ◽  
Tarun Chaudhary ◽  
Rishabh Arora ◽  
Shantanu Kumar Sahu

Gastrointestinal tumors (GIST) are malignant and rare forms of soft tissue sarcoma arising from interstitial cells of Cajal. With most common site of origin being stomach, Jejunal GIST accounts for 0.1–3% of all GIST. Due to non specific signs and symptoms diagnosis is often delayed and patient mostly presents in advanced stage. 50 year old female presented with decreased appetite from 5 months and lump in upper abdomen from 3 months associated with dull abdominal pain from 15 days. CECT abdomen showed a large soft tissue mass in left lumbar region. Exploratory laparotomy showed a highly vascular mass of size 12x10x8 cm abutting mesentery of transverse colon lodged between middle colic artery and superior mesenteric artery. Resection of mass with a segment of jejunum was done. Histopathological examination showed spindle cell tumor with high mitotic index with CD 117+. Adjuvant chemotherapy was given and patient is currently asymptomatic after 9 months of postoperative follow up. Spectrum of clinical presentation is broad so a preoperative diagnosis is difficult. GIST primarily presenting as an abdominal lump is rare and only 25 cases have been reported so far. Surgery is the primary mode of treatment but imatinib has transformed the treatment. Newer drugs are under phase II trials and hopefully will change the course of management in near future.


2021 ◽  
pp. 006-009
Author(s):  
Katsuva John Musubao ◽  
Vuhaka Simplice Kighoma ◽  
Vululi Sosthene Tsongo

The current case is one of the rare clinical presentations of the brachial artery pseudo aneurysm presentation in children Pseudo-aneurism is one of the late complications of a missed or untreated arterial injury. The diagnosis is suggested in the presence of clinical signs such as: an expending, ill-defined mass with or without pulsation; bruit, pain, paresthesia, or paralysis due to nerve compression. Although plain X-Rays may show a nonspecific soft tissue mass, arteriography is essential in defining differentiating pseudo aneurisms from other soft masses. We report a case of a 10years old boy with a history of a stab injury in a well vascularized left cubital fossa region. The physical examination revealed a soft tissue mass with eroded skin. Ultrasound and MRI findings were respectively of an infected soft tissue mass and probable malignant soft tissue mass. Open biopsy was planned but surgical finding revealed a pseudo aneurism of the left brachial artery before its bifurcation. Brachial arterial lesion was repaired blood flow reestablished with clinical improvement.


2019 ◽  
Vol 13 (Supl 1) ◽  
pp. 19S
Author(s):  
Danilo Ryuko Cândido Nishikawa ◽  
Ana Caroline Leite da Silva ◽  
Fernando Aires Duarte ◽  
Guilherme Honda Saito ◽  
Augusto César Monteiro ◽  
...  

Introduction: Eccrine poroma (EP) and poroid hidradenoma (PH) are rare benign neoplasms derived from eccrine sweat glands of the epithelium. Both are variants of poroid neoplasms and rarely become malignant. This report describes the clinical presentation, radiographic and pathological features as well as the treatment of a rare association of EP and PH in a large single lesion over the foot.  Case Report: We present a 55-year-old male patient with a large soft tissue mass over the midfoot (approximately 7 cm in length and 4 cm width). It started as a hyperchromic black spot on the skin and has slowly grown over the last eight years. One year prior, pain increased significantly. There was no history of trauma, infection or other tumor in this part of the foot. In the physical exam, the tumor had well-defined edges, fibroelastic consistency and was not adherent to the surrounding soft tissue. Preoperative planning included radiographic exams: X-ray and magnetic resonance imaging (MRI). On the MRI, the tumor showed a low signal intensity on T1-weighted images, with heterogeneous high and low signal intensities on T2-weighted images. Strong contrast enhancement was observed after intravenous gadolinium administration in the base portion. The peripheral portion showed a low signal intensity without enhancement. We decided on total resection, and the procedure was performed in January of 2017. The surgical approach was a longitudinal dorsomedial incision over the first ray starting from the ankle joint to the distal third of the first metatarsal. The entire tumor was excised with clean margins and sent for anatomopathological analysis and histopathological examination. Histopathologic examination showed that the tumor was a poroid neoplasm consisting of both dermis (poroid hidradenoma) and epidermis (eccrine poroma) components. There were no features of malignancy. After 20 months of surgery, patient remains asymptomatic with no signs of recurrence of the tumor. Conclusion: Skin tumors must be born in mind in the differential diagnosis of a chronic mass in the foot. Surgical treatment for this type of tumor is curative and prevents recurrence and malignant change.


2010 ◽  
Vol 12 (4) ◽  
pp. 334-337 ◽  
Author(s):  
Thomas J. Smith ◽  
Wendy I. Baltzer ◽  
Craig G. Ruaux ◽  
Jerry R. Heidel ◽  
Patrick Carney

An 11-year-old cat presented for evaluation of intermittent vomiting, constipation and hyporexia of 3 weeks duration. Ultrasonographic and endoscopic examination revealed a soft tissue mass adjacent to the lower gastro-esophageal sphincter. Surgical excision of the mass was successfully performed resulting in a resolution of clinical signs. Histologically the mass was consistent with a smooth muscle hamartoma. At follow-up 7 months after surgery, the cat remained free from clinical signs.


2018 ◽  
Vol 108 (2) ◽  
pp. 172-177 ◽  
Author(s):  
Dyane E. Tower ◽  
Jeffrey R. Hammond

Acral fibrokeratoma is a rare soft-tissue mass, more commonly found on the hands and rarely on the feet. This case report of a 40-year-old Hispanic man highlights an unusually located acral fibrokeratoma on the second toe, describes the clinical presentation and microscopic and pathologic findings, discusses differential diagnoses, and presents treatment options.


2017 ◽  
Vol 22 (01) ◽  
pp. 128-130 ◽  
Author(s):  
Adam M. Feintisch ◽  
Andrew A. Marano ◽  
Gregory L. Borah

A nonspecific soft tissue mass of the hand can be difficult to diagnose due to the multitude of possible etiologies. In this case, we discuss our experience in diagnosing and treating intravascular papillary endothelial hyperplasia, or Masson’s tumor, of the hand. The wide range of differential diagnoses and the morphological resemblance to angiosarcoma make Masson’s tumor an important clinical entity to understand. The purpose of this study is to familiarize the reader with the appropriate diagnostic and treatment modalities that allow the clinician to recognize Masson’s tumor, differentiate it from similar clinical entities, and institute the appropriate management regimen.


2017 ◽  
Vol 45 ◽  
pp. 5
Author(s):  
Fernanda Carlini Dos Santos ◽  
Lays Wouters Ugolini ◽  
Henrique Ramos Oliveira ◽  
Tanise Policarpo Machado ◽  
Leonardo Porto Alves

Background: Lymphoma, although rare, is the most common hematopoietic neoplasia in horses. The overall incidence of lymphoma is between 1.3-2.8% of all equine neoplasia and it has a prevalence of 0.002-0.5% in the equine population. Lymphoma can be classified as multicentric, alimentary, mediastinal, cutaneous and solitary. The cutaneous is the rarest form and it usually presents with multifocal skin lesions, with no other clinical signs. The diagnoses is accomplished by histopathological examination of a biopsy or cytological examination of a fine needle aspirate. The aim of the current study is to report a case of the rarest form of equine lymphoma, the cutaneous.Case: An 8-year-old equine female, Quarter Mile, was evaluated due to volume’s increase and subcutaneous nodules disseminated along the body. These lesions developed gradually during 2 years. The mare was used for ridding, it was kept in the field with 10 other equines and was the only one affected. The mare was vaccinated for influenza and was negative for glanders and equine infectious anemia. During clinical exam, all vital parameters were within limits and body condition score was classified as 6 (Henneke Chart). It was observed bilateral nasal secretion and depigmentation in ocular and vulvar mucous. It was observed multiple delimited areas with size ranging from few cm up to 7 cm, hard, mobile, painless, located in the subcutaneous and disseminated in the body (including head, neck, thorax, limbs and perineum). Red blood cell, leucocytes, fibrinogen, total plasmatic protein were within normal limits. Due to clinical signs and the potential risk of a zoonosis, the glanders test was repeated (complement fixation test) and the result was negative. Differential diagnoses also included insect hypersensitive, which was discarded since the female did not presented pruritus nor alopecia, lesions gradually increased in size and no seasonality was observed. It was performed excisional biopsy for tissue culture, which revealed no growth of aerobic mesophile bacteria. Histopathological evaluation revealed rounded cell proliferation similar to lymphocytes situated in the deep derma and subcutaneous. After evaluation of history, clinical exam and complementary exams the mare was diagnosed with cutaneous lymphoma. The owner was instructed that there was no available specific treatment with good efficacy and viable for equines at this stage. Besides, it is important to evaluated the mare constantly due the possibility of future lesions in organs or intern lymph nodes.Discussion: Cutaneous lymphoma is an uncommon disease, especially in horses, that can present with variable clinical signs, immunosuppression, rapid systemic disease progression or none at all. In the present case report, during clinical examination lesions were observed in areas of lymphatic drainage. Identification of neoplastic lymphocytes during cytological examination or histopathological evaluation of biopsy tissue can confirm the presence of lymphoma, as performed in the present case. Treatment is palliative and occasionally results in complete cure, mainly in equine with single lesions. The mare had cutaneous lymphoma disseminated all long the body and no clinical signs that could suggest gastrointestinal neoplastic lesions, even though the owner was advised that this animal should be monitored regularly in the future, specially due the possibility of metastatic lesions in any other organ. In equine, lymphoma has low incidence and the cutaneous form is the rarest one. Clinical signs are typically non specific and develop insidiously, so it is important to perform complementary exams for accurate diagnoses and for differential diagnoses of tegumental and infectious diseases.


2021 ◽  
Vol 0 ◽  
pp. 1-4
Author(s):  
Nagendra Mishra ◽  
Henil Upadhyay ◽  
Charmy Parikh

Actinomycosis is a rare chronic granulomatous suppurative infection caused by Gram-positive bacteria. The occurrence of primary vesical actinomycosis is extremely rare and only a few cases have been reported. Pre-operative diagnosis of vesical actinomycosis is challenging as the clinical and radiological features usually point towards bladder malignancy. Therefore, in most cases, definitive diagnosis is usually made after histopathological examination of the involved tissue. A 60-year-old male presented with complaints of hematuria, burning micturition, irritative, and obstructive urinary symptoms for 15 days. USG revealed a large soft-tissue mass having a polypoidal intraluminal and extraluminal component and involving the right posterolateral urinary bladder wall. CT scan showed a large irregular soft-tissue mass with multiple cystic lesions involving the right lateral wall of the urinary bladder. Transurethral resection of bladder mass biopsy was performed and the histopathological examination showed bacterial colonies of Actinomyces with changes of cystitis cystica. The patient was treated with amoxicillin and potassium clavulanate for 3 months. Actinomycosis should be kept as a rare differential diagnosis in cases presenting as bladder mass. The diagnosis is most commonly made by histopathology and may need a repeat biopsy to arrive at the correct diagnosis. The patient should be treated by penicillin group of antibiotics for 2–3 months and followed up for years to detect any recurrence.


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