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Renal cell carcinoma with cutaneous metastasis:

case report

Authors

Thaís Alves de Paula1 Polyana Souto Lopes da Silva1

Luiz Gustavo Sueth Berriel1

1Hospital Ipiranga –

Ave-nida Nazaré, 28, Ipiranga, São Paulo- SP - Brazil

Submitted: 05/25/2009 Accepted: 10/20/2009

Correspondence to: Thaís Alves de Paula Rua Ouvidor Peleja, 98, ap. 131

Vila Mariana – São Paulo, SP, Brasil

CEP: 04128-000

E-mail: tatyalp@gmail.com

We declare no confl ict of interest.

A

BSTRACT

Renal cell carcinoma or hypernephroma is the third most common neoplasia of the genitourinary tract. Its most common type, representing 60% of the cases, is the clear cell carcinoma, with an incidence peak between 50 and 70 years. Metas-tases are present at the time of diagnosis in approximately 30% of the patients, the major sites being lungs, bones, skin, liver, and brain. We report the case of a male patient with renal cell carcinoma, whose age, clinical findings, and tumor histologi-cal type matched with the most common ones for that pathology. Nevertheless, he already had distant metastasis in an un-common site at the time of diagnosis. The patient died without undergoing specific treatment for renal cell carcinoma. Keywords: renal carcinoma, cutaneos me-tastasis.

[J Bras Nefrol 2010;32(2):213-215]©Elsevier Editora Ltda.

I

NTRODUCTION

Carcinoma of the kidney, also known as renal adenocarcinoma, renal cell car-cinoma, or hypernephroma, accounts for approximately 2% of the cancers in adults, and affects more men than women (1.5:1).4,5,9,10 Renal clear cell carcinoma

is its most frequent type.9 It is the third

most common neoplasia of the genitou-rinary tract, after prostate and ugenitou-rinary bladder tumors. At diagnosis, one third of the patients usually have distant me-tastases. The most common sites are lungs (50%), bones (33%), skin (11%), liver (8%), and brain (3%).4,6,7 We report the

case of a male patient with renal cell car-cinoma, whose age, clinical findings, and

tumor histological type matched with the most common ones for that pathology. Nevertheless, he already had distant me-tastasis in an uncommon site at the time of diagnosis.

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214 J Bras Nefrol 2010;32(2):213-215

clear cell carcinoma. After two months, the patient sought the Hospital Ipiranga again, complaining of severe dyspnea, inappetence and lower limb edema. The chest radiography showed a significant pleural effusion to the right and multiple pulmonary nodu-les. The patient was admitted due to a picture of de-compensation, and diagnostic thoracocentesis with pleural biopsy was performed. The effusion was he-morrhagic, but was characterized as transudate. The pleural biopsy showed only an inflammatory pattern. Despite all measures, the patient developed acute res-piratory failure and died, without undergoing specific treatment for renal cell carcinoma.

D

ISCUSSION

Renal cell carcinoma has its incidence peak betwe-en 50 and 70 years of age (mean age, approximately 66 years) and prevails in the male sex (2:1). In the past 25-30 years, its incidence increased considerably partially due to the improvement in imaging diag-nosis, being currently around 2 to 10 cases/100,000 inhabitants/year. Its major etiologies are as follows: tobacco, cystic disease, tuberous sclerosis, and von Hippel-Lindau syndrome. The major type of renal cell carcinoma is that of clear cells, representing 60% of the cases. The initial clinical findings comprise hematuria (60%), lumbar pain (40%), and palpa-ble flank mass (30-40%). In addition, the following may be found: fever, weight loss, anemia, varicocele, and paraneoplastic syndromes (5%) characterized by erythrocytosis, hypercalcemia, liver dysfunction, and amyloidosis.7,9,10 The classic triad comprising

abdo-minal mass, hematuria, and pain is present in only 10% of the cases, and usually in more advanced sta-ges with poor prognosis.4,7,9,10 The diagnosis is

esta-blished through image tests, such as ultrasound and computed tomography of the abdomen, with diagno-sis sensitivity of 79% and 94%, respectively, in addi-tion to chest X-rays, urinalysis and urinary cytology. Magnetic resonance imaging is indicated when invol-vement of the vena cava or its invasion by a thrombus is suspected. The most common sites of metastases are as follows: lungs (50%), bones (33%), regional lymph nodes and skin (11%), liver (8%), adrenal gland and brain (3%).4,6,7

Regarding the cutaneous metastasis of renal car-cinoma described in the literature, the most common site was the scalp, followed by the abdominal region.1

The scalp is a frequent site of cutaneous metastasis of distant primary tumors. It is the major or sole site of metastases originating from several organs, such

as rectum, breast, lung, uterus, prostate, testis, uri-nary bladder, and kidney. In men, the primary tu-mor of a scalp metastasis is frequently located in the lung or kidney, as in the clinical case reported. In women, the primary tumor of a scalp metasta-sis is frequently located in the breast. Krumerman & Garret2 may have explained this fact by stating

that highly angioinvasive tumors, such as lung and renal cancers, tend to originate unlimited, early me-tastases, with an unpredictable pattern of location, usually far away from the primary tumor. The most frequent clinical appearance of cutaneous metasta-ses is that of intra- or subcutaneous, round or oval, nodular masses, of firm or elastic consistency, and highly varied color, ranging from normal skin co-lor, bluish red or purplish, similar to that of our patient, to dark brown.

Regarding the histopathology of renal clear cell carcinoma, the tumor cells are polyedric with abun-dant cytoplasm, atypical nucleus, and evident nu-cleolus. In the metastatic dermal lesion, the nodular tumor is covered by atrophic epidermis, with tumor cells of vacuolar appearance, clear cytoplasm, mild lymphocytic inflammatory infiltrate, abundant ca-pillary formation, and some trabecular areas. A small epidermal invagination delimits the lesion from the normal dermis.8

Some protein antigens are evidenced by use of im-munohistochemistry, such as the epithelial membrane antigen (EMA), vimentin, keratin, and carcinoem-bryonic antigen (CEA). The positive results with vi-mentin, EMA, and keratin are high-probability indi-cators of renal cell carcinoma.8

The differential diagnoses of renal lesions are as follows: angiomyolipoma; transitional cell carcinoma of the renal pelvis; adrenal gland tumor; and renal abscess. Regarding the cutaneous lesion, the differen-tial diagnoses are as follows: sebaceous carcinoma; sweat gland tumor; and melanoma.10

In the absence of metastases, surgical removal of the affected kidney and lymph nodes provides a good probability of cure. When the tumor has alre-ady invaded the renal vein or the vena cava, but has not produced distant metastases, surgery may provi-de a chance of cure. However, renal cancer has a ten-dency to early dissemination, especially to the lungs. When renal cancer has already produced metastases, its prognosis is poor, because it can be cured with neither radiation therapy, nor traditional antineo-plastic drugs (chemotherapy), nor hormones.4,8 Our

patient died without undergoing specific treatment for renal tumor.

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J Bras Nefrol 2010;32(2):213-215

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EFERENCES

1. Brownstein MH, Helwig EB. Patterns of cutaneous me-tastasis. Arch Dermatol 1972; 105: 862-8.

2. Krumerman MS, Garret R. Carcinomas metastatic to skin. NY State J Med 1977; 77(12)1900-3.

3. Rosen T. Cutaneous metastases. Med Clin North Am 1980; 64(5):885-90.

4. Linehan MW, Cordon-Cardo C, Isaacs W. Cancers of Genitourinary System. In: DeVita, VT, Hellman, S, Rosenberg, SA. Cancer: principles & practice of onco-logy, 5 ed. Philadelphia: JB Lippincott, 1997:pp 1253-70.

5. Sittart JAS, Criado PR, Gomes MI, Ananias MTP. Metástases cutâneas de carcinomas internos. Med Cut I LA 1995; 23:11-4.

6. Bordin GM, Weitzner S. Cutaneous metastases as a manifestation of carcinoma: diagnostic and prognostic significance. Am Surg 1972; 38(11):629-34.

7. Wahner-Roedler DL, Sebo TJ. Renal Cell Carcinoma: diagnosis based on metastatic manifestations. Mayo Clin Proc 1997; 72(10):935-40.

8. Kouroupakis D, Patsea E, Sofras F. Apostolikas N. Renal cell carcinoma metastasis to the skin: a not so rare case? Brit J Urol 1995; 75(5):583-5.

9. Goldman L, Bennett JC. Cecil – Tratado de Medicina Interna, 21 ed. 2001; pp700-2.

10. Hugo HS. Cancer. In: McPhee SJ, Papadakis MA, edi-tors. Current medical diagnosis and treatment, Chapter 39, 48th ed. 2009: pp 1463-4, 1489-90.

Referências

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