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2016, Number 2

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Dermatología Cosmética, Médica y Quirúrgica 2016; 14 (2)

Porocarcinoma: clinical-histopathologic features and Ki-67 proliferative index. Study of 24 cases

Barrera JA, Moreno LLM, Peniche CA, Mercadillo PP
Full text How to cite this article

Language: Spanish
References: 7
Page: 119-126
PDF size: 334.54 Kb.


Key words:

porocarcinoma, Ki-67 proliferation index, local recurrence, metastasis, mortality.

ABSTRACT

Porocarcinoma is a malignant proliferation originated from intraepidermal portion of eccrine glands. Its frequency is rare as it represents less than 1% of cutaneous tumors.
Our objective is to report the clinical-histophalogical characteristics of all the 24 cases registered in the Dermatopathology Unit from Hospital General de Mexico “Dr. Eduardo Liceaga”, from January 1975 to December 2013, and to measure the semi-quantitative Ki-67 protein expression, a well known proliferation index and to correlate its expression with the clinical outcome in each patient.
We found porocarcinoma more frequently in women (ratio 2:1), with a mean age 59.7 (range 18 to 87 years). The most frequent localization on the lower limbs, with a predominant nodular morphology and a mean clinical size of 2.3 cm. Histopathological characteristics showed that most of the cases were invasive 23, (95.8%), with duct formation 18 (75%) and associated to a benign eccrine poroma 11 (45%). Mean histological depth, 3.46 mm and all biopsies had immunohistochemistry epithelial membrane antigen and carcinoembrionary antigen with a variable expression, as Ki-67 protein expression, had a wide range from 5 to 80% of total lesion and statistical analysis showed a significant relationship between Ki-67 expression and local recurrence, invasion, metastasis and death due to porocarcinoma.
We conclude that the high expression of Ki-67 proliferation index is a poor prognostic factor in patients with porocarcinoma as it represents a higher probability of local recurrence, invasion, metastasis and mortality. So we proposed the routinary determination of this proliferation index in order to obtain a complete histological and immunohistochemical evaluation of porocarcinoma.


REFERENCES

  1. Goel, R., Contos, M.J. y Wallace, M.L., “Widespread metastatic eccrine porocarcinoma”, J Am Acad Dermatol, 2003, 49: S252-254.

  2. Mercadillo-Pérez, P, Morales-Trujillo, M.L., Moreno-López, L.M. y Peniche-Castellanos, A., “Porocarcinoma ecrino. Reporte de un caso”, Rev Hosp Gen Mex, 2010, 73: 29-42.

  3. Brown, Jr., C. y Dy, L.C., “Eccrine porocarcinoma”, Dermatol Ther, 2008, 21: 433-438.

  4. Requena, L., Kutzner, H., Hurt, M.A., Santa Cruz, D.J. y Meheregan, A.H., “Malignant tumours with apocrine and eccrine differentiation”, en LeBoit, P., Burg, G., Weedon, D. y Sarasin, A. (eds.), Pathology and genetics. Skin tumours. World health organization classification of tumours, Lyon, World Health Organization, 2006: 128-130.

  5. Lever, W. y Schaumburg-Lever, G., “Poroma ecrino maligno”, en Lever, W. (ed.), Histopatología de la piel, Buenos Aires, Intermédica, 1991, pp. 574-575.

  6. Robson, A., Greene, J. y Ansari, N., “Eccrine porocarcinoma: a clinicopathologic study of 69 cases”, Am Surg Pathol, 2001, 25: 710-720.

  7. Chang, O., Elnawawi, A., Rimpel, B., Asarian, A. y Chaudrhy, N., “Eccrine porocarcinoma of the lower extremity: a case report and review of literature”, World J Surg Oncol, 2011, 9: 94-97.




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Dermatología Cosmética, Médica y Quirúrgica. 2016;14