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Vet Pathol 30:3, 1993 Brief Communications and Case Reports 313

References 5 Mayr B, Swidersky W, Schleger W: Translocation t(4;27)


in a canine mammary complex adenocarcinoma. Vet Rec
Hampe JF, Misdorp W: IX, Tumors and dysplasias of
126:42, 1990
the mammary gland. Bull WHO 50: 111-133, 1974
6 Selden JR, Moorhead PS, Oehlert ML, Patterson DF: The
2 Mayr B, Schleger W, Kalat M, Schweiger P, Reifinger M, Giemsa banding pattern of the canine karyotype. Cyto-
Eisenmenger E: Cytogenetic studies in a canine mammary
genet Cell Genet 15:380-387, 1975
tumor. Cancer Genet Cytogenet 47:83-87, 1990
7 Wang HC, Fedoroff S: Banding in human chromosomes
3 Mayr B, Schleger W, Swidersky W, Loupal G: Isochro-
treated with trypsin. Nature New Bioi 235:52-54, 1972
mosomes 13 in a canine osteochondrosarcoma in the
mammary region. J Small Anim Pract 31:407, 1990
Request reprints from Dr. B. Mayr, Institute for Animal
4 Mayr B, Schweizer D, Schleger W: Characterization of
Breeding and Genetics, Veterinary University, Linke Bahn-
the canine karyotype by counterstain enhanced chromo-
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some banding. Can J Genet Cytol 25:616-621, 1983

Vet Patho1 30:313-314 (1993)

Complex Adnexal Tumor with Sebaceous and Apocrine Differentiation in a Guinea Pig

N. ALLISON AND R. MOELLER, JR.

Key words: Guinea pigs; neoplasia; skin; tumor.

A 3-year-old female guinea pig was examined because of have differentiated into larger cells with pink cytoplasm, which
a swelling in the right inguinal area that had been present for contained multiple discrete vacuoles. These cells blended in
several months. A 2.7- x 1.5-cm x 1.5-cm mass was sur- with large adiposites that had distinct cytoplasmic borders,
gically excised. The mass was distinctly bilobed; the larger colorless cytoplasm, and small dark crescentic to plump open-
lobe was pale and soft, and the smaller lobe was firm and faced ovoid nuclei (Fig. 2). Mitotic figures were rarely seen
pink. The specimen was fixed in 10% neutral buffered for- in this lobe, and then only in the tubular component. The
malin and processed routinely, and sections were embedded neoplasm was judged to be benign because it was well cir-
in paraffin and stained with hematoxylin and eosin. cumscribed and the neoplastic cells were well differentiated.
Histologically, the mass was well circumscribed, nonen- This tumor was difficult to classify. It had many features
capsulated, and separated into two distinct lobes bordered of a complex mammary tumor; however, mammary gland
by compressed adipose tissue and loose connective tissue; neoplasms do not have a sebaceous component. According
overlying skin was not present. The smaller of the two lobes to the World Health Organization classification of tumors,
was composed of poorly to well-defined sebaceous glands complex tumors are composed ofboth secretory and myoepi-
and tubular or ductal structures separated by a prominent thelial components.' This neoplasm contained both a secre-
spindle cell component (Fig. I). Many ducts were dilated, tory component and myoepithelial component, with differ-
and a few were cystic. Small papillary projections extended entiation of the myoepithelial component into adipocytes.
into the lumina of the cystic ducts. Most ofthe tubular/ductal Therefore the diagnosis was benign, complex, adnexal tumor
component was lined by a tightly packed inner layer of cu- with sebaceous and apocrine differentiation.
boidal to columnar epithelium, with eosinophilic cytoplasm The most plausible explanation of the origin of this neo-
and occasional apical blebs. An inconspicuous outer layer of plasm is that it arose from an epithelial pleuropotential cell
slender to plump spindle cells, resembling myoepithelium, that differentiated into sebaceous, apocrine, and myoepithe-
surrounded the ducts and blended into the stroma. A few lial cell progenitors. Although this neoplasm could have been
ducts associated with sebaceous glands were lined by strat- classified as a complex mammary gland adenoma with en-
ified squamous epithelium. The stroma was highly cellular trapped sebaceous glands, this explanation is unlikely be-
(interpreted to be of myoepithelial origin) and consisted of cause the sebaceous glands were in the subcutis where such
moderately pleomorphic cells with indistinct cytoplasmic glands are not normally found. Also, the compressive nature
borders, pale eosinophilic cytoplasm, and ovoid to spindle- of the mass suggests that if any ectopic sebaceous glands had
shaped open-faced nuclei with blunt ends; some nuclei were been present, the glands would have been pushed aside by
slightly twisted. A few areas of stroma had a loose myxoid the expanding mass. Another explanation considered was
appearance (Fig. I). Mitotic figures were common in both that one lobe of the mass represented a complex adnexal
the glandular and stromal components but were more nu- tumor that had collided with a lipoma with entrapped se-
merous in the stroma. The larger lobe contained a few ran- baceous and apocrine components. This explanation is also
domly distributed sebaceous and tubular structures sur- unlikely. The close association of slender spindle cells, which
rounded by spindle cells (myoepithelium) that appeared to resembled those surrounding the apocrine component of the
314 Brief Communications and Case Reports Vet Pathol 30:3, 1993

Fig. 1. Skin tumor; guinea pig. Sebaceous (S) and ductal structures (arrows) surround a prominent spindle cell component
(asterisk) with myxoid area (M). HE.
Fig. 2. Skin tumor; guinea pig. Cells with pink cytoplasm containing mlutiple discrete vacuoles of various sizes (arrow-
head) lie adjacent to other cells with distinct cytoplasmic borders, colorless cytoplasm and eccentric nuclei (A). HE.

mass (myoepithelium), plumper cells, which contained pink 2 Ediger RD, Kovatch RM: Spontaneous tumors in the
cytoplasm with multiple discrete vacuoles of various sizes, Dunkin-Hartley guinea pig. Ann Natl Cancer Inst 56:
and large adipocytes, with clear cytoplasm and eccentric nu- 293-294, 1976
clei, suggests that these cells were of a common origin. Elec- 3 Hampe JF, Misdorp W: Tumors and dysplasias of the
tron microscopic examination and immunohistochemical mammary gland. Bull WHO 50: 111-133, 1974
studies may have been useful in further elucidating the iden- 4 Kitchen DN, Carlton WW, Bickford AA: A report of
tity and relationship of the different cell populations, but fourteen spontaneous tumors of the guinea pig. Lab Anim
sufficient tissue of acceptable quality was not available for Sci 25:92-102, 1975
such studies. 5 Lever WF, Schaumburg-Lever G: Histopathology ofthe
A search of the literature failed to identify any neoplasms Skin, 6th ed., p. 524. JB Lippincott Co, Philadelphia,
with similar characteristics in other animals. In human be- PA, 1983
ings, a neoplasm with both apocrine and sebaceous glands 6 Lombard C: La cancero-resistance du cobaye. Bull Assoc
and a myoepithelial component has been described. How- FrEtudeCancer47:167-171,1961
ever, this neoplasm also had a prominent epidermal com- 7 Mosinger M: Sur 1a carcinoresistance du cobaye. Pre-
ponent ofacanthosis and papillomatosis, which was not pres- miere partie. Les tumeurs spontanees du cobaye. Bull
ent in the tumor from this guinea pig.'? Assoc Fr Etude Cancer 47:217-235, 1961
Tumors of the epidermis and adnexa have been infre- 8 Murray JA: A transplantable sarcoma of the guinea pig.
quently reported in the guinea pig. Trichofolliculoma is the J Pathol Bacterio1 20:260-268, 1916
most common skin tumor of this species. 1,2,9,11 Trichoepi- 9 Tuck E, Tuck K: Trichofolliculorn beim Meer-
thelioma has also been reported in the guinea pig.4 However, schweinchen. Kleintierpraxis 24:237-238, 1979
these neoplasms were described as having abortive adnexal 10 Wechsler HL, Fisher ER: A combined polymorphic epi-
structures in the wall of cysts lined by stratified squamous dermal and adnexal tumor in nevus lateralis. Derma-
epithelium," which are features oftrichofolliculoma. 4- 8 , 1 1 This tologica (Basel) 130:158-164,1964
is the first reported case of a complex adnexal tumor in the 11 Zwart P, Van de Hage MH, Mullink JWMA, Cooper JE:
guinea pig. Cutaneous tumours in the guinea pig. Lab Anim 15:375-
377, 1981
Acknowledgement
We thank Dr. G. McGrath for submitting the case to us. Request reprints from Dr. N. Allison, Virginia Department
of Agriculture and Consumer Services, Pathology Reference
References Laboratory, Room 162, 1 North 14th Street, Richmond, VA
23219 (USA).
Ediger RD, Dill GS, Kovatch RM: Trichofolliculoma
of the guinea pig. J Natl Cancer Inst 46:517-523, 1971

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