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Two types have been observed in dogs and one in cats; neither type has 622 Epithelial neoplasms and other tumors an exact human analogue heart attack kiss the way we were goodbye buy 2.5mg zestril overnight delivery. A small number of cases have been described in the literature (Diters & Goldschmidt blood pressure medication vivid dreams purchase zestril 10mg without a prescription, 1983; Walsh & Corapi arrhythmia fatigue buy 10 mg zestril visa, 1986; Scott & Anderson blood pressure testing cheap zestril 2.5 mg with amex, 1991). These lesions present as firm, circumscribed nodules, ranging from 1 to 7 cm in diameter, that are most often located on the head and neck. The average age of affected animals is 10 years, and there does not appear to be any breed predisposition. A second type of tricholemmoma resembles the outer root sheath of the isthmus segment of the follicle, particularly as it appears during catagen phase. Within each lobule epithelial cells are arranged in islands, nests, and delicate trabeculae. The epithelial aggregates are cuffed by thick, glassy, basement membrane zones reminiscent of the vitreous sheath of normal hair follicles. The majority of cells have clear cytoplasm, and there is prominent peripheral palisading. The cells in the centers of the islands may have more abundant, eosinophilic cytoplasm, and there may be small foci of keratinization without keratohyalin or trichohyalin granules. Nuclei are small, ovoid, and euchromatic; nucleoli are inconspicuous, and mitotic activity is low. Differential diagnoses for inferior tricholemmoma are limited, as cutaneous tumors composed predominantly of. Islands and nests of very pale epithelial cells form a large dermal mass with a pale fibrous stroma. The rare clear cell variant of basal cell carcinoma generally has larger cells and larger cell aggregates than tricholemmoma. Granular cell trichoblastoma has more cords and nests than islands and trabeculae, although the granular cells may appear almost clear. The nuclei of tricholemmoma are not peripherally displaced as they are in granular cell trichoblastoma. Tumors that are otherwise typical for ribbon trichoblastoma occasionally have areas resembling bulb tricholemmoma with transition between hair germ and outer root sheath morphology. Note prominent basement membranes resembling vitreous sheaths around some of the epithelial aggregates (arrow). Islands and trabeculae of small, pale keratinocytes in a bland fibrous stroma form a wellcircumscribed dermal mass. Cords and trabeculae of epithelial cells radiate outward from large epithelial islands and often interconnect adjacent islands. The centers of the islands have small foci of tricholemmal-type keratinization (without formation of keratohyalin or trichohyalin granules). Larger islands may have a pseudocystic appearance due to drop-out of all of the central keratin. There is a moderate collagenous stroma of low cellularity; small amounts of mucin may be present. Neoplastic cells are fairly small, cuboidal to rounded, and have moderate, pink, often glassy cytoplasm. Nuclei are small, ovoid, and euchromatic with inconspicuous nucleoli and low mitotic activity. Scattered shrunken cells with condensed cytoplasm and small hyperchromatic nuclei may be present; these may represent either apoptosis or dyskeratosis (premature cornification of individual cells). Mild melanization of the epithelial cells may be present; occasional lesions are heavily melanized. Differential diagnoses for isthmic tricholemmoma are limited, as few known tumors are composed almost entirely of small, pink epithelial cells. Infundibular keratinizing acanthoma has some similar features, but is distinguished from isthmic tricholemmoma by the presence of a well-defined central cyst, multiple secondary cysts and abundant stromal mucin. Trabecular trichoblastoma may have a similar overall architecture, but is differentiated from isthmic tricholemmoma by the presence of prominent peripheral palisading, some spindling of epithelial cells, and predominance of smaller, prismatic keratinocytes. Multiple islands of pale keratinocytes contain central cysts filled with amorphous keratin and melanin pigment.
Eosinophilic plaque may have striking epidermal and follicular mucinosis heart attack burger discount 10 mg zestril visa, which is generally not a feature of miliary dermatitis blood pressure medication leg swelling cheap zestril line. Superficial pustular pyoderma (impetigo) is rare in cats arteria epigastrica cranialis superficialis cheap 2.5 mg zestril, but crusts formed from chronic Ulcerative and crusting diseases of the epidermis 121 pustules may be reminiscent of miliary dermatitis hypertension 15090 purchase zestril 5mg overnight delivery. Miliary dermatitis features dermal eosinophilic inflammation more prominently than most cases of impetigo, and also can exhibit transepithelial migration of eosinophils, a rare occurrence in pyoderma. The ulcer bed is covered by a crust that is brightly eosinophilic, due to the presence of degenerating eosinophils. Mild to severe spongiosis and/or mucinosis with eosinophilic exocytosis also extends to the superficial follicular epithelium (see Chapter 5). Multiple, well-demarcated, ulcerated, erythematous plaques are present on the ventral abdomen of a cat with allergic miliary dermatitis. Diffuse severe dermal inflammation lies beneath extensive ulceration and exudation. Pallor of the remaining superficial follicular epithelium is due to spongiosis and mucinosis. A striking, welldemarcated, erythematous lesion with swelling, alopecia, erosion, ulceration, and exudation has developed rapidly on the dorsal muzzle. Dermal inflammation consists of variably intense, usually diffuse infiltrations of eosinophils, which extend to the middle (follicular) dermis, but also commonly reach the superficial panniculus (see Chapter 14). The severe ulceration and depth of eosinophilic inflammation of some eosinophilic plaques may resemble feline mosquito bite hypersensitivity, feline indolent ulcer (eosinophilic type), and feline herpesvirus ulcerative dermatitis (eosinophilic type). The diffuse prominent spongiosis and mucinosis of typical eosinophilic plaque are not observed in these other conditions. Eosinophilic degranulation, or flame figure formation, is not observed in eosinophilic plaque, as in the other diseases (see Chapter 14). Lesions have been documented to occur at the exact site of previous mosquito bites (Mason & Evans, 1991). It is not known if the same reaction pattern can be seen with the bite of other flying insects. The clinical and histologic features of this syndrome were described before the etiology was known (Wilkinson & Bates, 1982). Similar to mosquito bite allergy in humans, allergy in cats likely involves both immediate and delayed hypersensitivity. Concomitant delayed hypersensitivity has been inferred by the clinical reaction pattern (Nagata & Ishida, 1997). The syndrome follows the classic seasonal pattern of mosquito bite hypersensitivity in humans, characterized by development of lesions in the summer and regression during autumn (Wilson & King, 1999). Further, the syndrome has been seen predominantly in cats allowed outdoors, and lesions resolve when strict indoor confinement is instituted (Mason & Evans, 1991). Diagnosis of feline mosquito bite hypersensitivity is highly regional; frequency of occurrence varies from uncommon in most areas to endemic in some locales. Highly variable frequency of occurrence among different geographic regions that support mosquito populations suggests that only some species of mosquito may induce hypersensitivity. In humans, mosquitoes display preference for darker skin over lighter skin, younger over older skin, warmer over cooler skin, and scented over unscented victims (Wilson & King, 1999). Similarly, preference for darker hair coat or skin color occurs in cats (Nagata & Ishida, Ulcerative and crusting diseases of the epidermis 123 1997). In one study in Japan, many more cats displayed darker coat coloring on the pinnae than the muzzle; the pinnae were affected more frequently (Nagata & Ishida, 1997). The affected body regions also are relatively less haired and thus presumably are attractive targets for flying insects. The most common clinical feature of feline mosquito bite hypersensitivity may be miliary dermatitis affecting both pinnae (Nagata & Ishida, 1997). However, this clinical presentation is less visually distinctive, and clinicians are less likely to biopsy pinnae. A partially symmetrical, erythematous facial eruption with papules and crusting may precede the more severe and characteristic lesions of rapidly progressive, strikingly well-demarcated, bilaterally symmetric facial swelling, alopecia, erosion, ulceration, and exudation (Ihrke & Gross, 1995). Hyperpigmentation or hypopigmentation may be sequela to active disease, and firm, hyperpigmented nodules may be present in chronic cases. Disease may be more widespread, and may affect the flexor surfaces of the carpi and the junction of pawpads and adjacent skin (Power & Ihrke, 1995).
Occasional phagocytic vacuoles contain neutrophils or cellular fragments of tumor cells arrhythmia generator purchase cheapest zestril. Neutrophils are consistently seen prehypertension 38 weeks pregnant purchase cheapest zestril, in particular in conjunction with areas of necrosis arrhythmia heart attack cheap zestril 5mg fast delivery. The number of reactive lymphocytes varies; occasional to numerous dispersed lymphocytes or aggregates of lymphocytes can be observed blood pressure control cheap zestril 2.5mg visa. Canine spindle cell predominant histiocytic sarcomas can mimic other pleomorphic spindle cell or round cell sarcomas, including poorly-differentiated fibrosarcomas (some of which may be of myofibroblastic origin), malignant peripheral nerve sheath tumors, pleomorphic leiomyosarcomas, pleomorphic liposarcomas, synovial cell sarcomas, and hemangiopericytomas. Some histiocytic sarcomas may have numerous giant cells and thus may require differentiation from anaplastic sarcomas with giant cells of variable origin (see Chapter 33). Fibrosarcomas are usually characterized by a more monomorphic spindle cell population than histiocytic sarcomas, and round tumor cells are uncommon. The presence of palisading tumor cells, occasional arrangement of the tumor cells in Antoni type A or B patterns, and the formation of Verocay bodies separate peripheral nerve Histiocytic tumors 851 sheath tumors from histiocytic sarcomas. In contrast to histiocytic sarcomas, peripheral nerve sheath tumors are ultrastructurally characterized by a basal lamina around the tumor cells that is often thickened and folded. Leiomyosarcomas arise from either the arrector pili muscles or from dermal vessel walls, and a connection with these structures may be evident. Pleomorphic leiomyosarcomas with giant cells may require differentiation from histiocytic sarcomas by immunohistochemistry (see below). Pleomorphic liposarcomas may be difficult to differentiate from histiocytic sarcomas, particularly if distinctly vacuolated lipoblasts are not evident. Similar to histiocytic sarcomas, synovial cell tumors may be composed of spindle-shaped and round tumor cells. In most cases, both pleomorphic liposarcomas and synovial cell sarcomas require immunohistochemistry to differentiate them from histiocytic sarcoma. Histiocytic sarcomas lack the perivascular arrangement seen in hemangiopericytomas. In contrast to histiocytic sarcomas, which originate in the subcutis and may extend into the dermis, Langerhans cell histiocytosis arises in the dermis, infiltrates the epidermis and extends into the subcutis. Poorly granulated mast cell tumors are separated from histiocytomas by the usual presence of small numbers of intracytoplasmic metachromatic granules, identified with Giemsa or toluidine blue stains. In: Veterinary Dermatopathology: A Macroscopic and Microscopic Evaluation of canine and Feline Skin Disease (T. However, in view of the diversity of the dendritic cell populations, histiocytic sarcomas in other visceral locations may arise from other subsets of dendritic cells. The exact subset of dendritic cells in feline histiocytic sarcoma remains to be determined. Solitary and multiple mast cell tumors, and cutaneous and systemic mastocytosis have been recognized in dogs and cats. The highest mast cell density in normal canine and feline skin is found in the perivascular dermis, while few mast cells can be found in the subcutaneous tissue. Compared to other body locations, mast cells are more numerous on the pinnae and the chin in dogs, and the pinnae and feet in cats (Foster, 1994; Auxilia & Hill, 2000). Mast cell precursors migrate from the bone marrow via blood into peripheral tissues where they differentiate into mature mast cells. Murine mast cells were initially classified into connective tissue (typical) mast cells and mucosal (atypical) mast cells based on the morphology of their granules, tinctorial properties, formaldehyde resistance, and granular components. Canine mast cells, similar to human mast cells, cannot be classified according to the system used in mice (Hill & Martin, 1998; Hill, 2002). This variation must be considered when immunohistochemistry for tryptase is used to identify canine mast cells. There is no equivalent characterization of feline cutaneous mast cells available to date. Similar to humans, canine mast cell tumors have been associated with mutations of the protooncogene c-kit, characterized by tandem duplications (London et al. This results in consistent activation of the receptor tyrosine kinase and subsequent mast cell proliferation. Similar mutations of the c-kit proto-oncogene were not found in splenic mast cell tumors of cats (London, C.
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