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Texte intégral de l'article
 
  Version imprimable

Multiple cutaneous metastases as the first sign of lung cancer in a patient with well-differentiated papillary transitional cell carcinoma of the urinary bladder


European Journal of Dermatology. Volume 8, Numéro 8, 573-4, December 1998, Cas cliniques


Summary  

Auteur(s) : J. Pec, L. Plank, J. Kliment, J. Luptak, E. Hajtmanova, M. Pec, St. Martin’s University Hospital, Jessenius Faculty of Medicine, Comenius University, Kollarova 2, 036 59 Martin, SK – Slovak Republic..

Illustrations

ARTICLE

Cutaneous metastases can be found in about 1 to 12% of patients with lung cancer [1, 2]. About 30% of these pulmonary cutaneous metastases show histological patterns of adenocarcinoma, 30% squamous cell carcinoma and 40% undifferentiated carcinoma [3]. Cutaneous metastases of small-cell carcinoma are much less common [4]. The presentation of cutaneous metastases as the first manifestation of lung cancer is very rare. In a large review of Lookingbill et al. [5], skin involvement was the first sign of cancer in 0.8% of systemic cancer patients.

We describe a rare case of lung cancer with cutaneous metastases as the first sign of the disease.

Case report

A 75-year-old man, a smoker (50 cigarettes per day for 55 years), had worked as a miner in uranium mines. In 1984, he had a Bilroth I a stomach resection for a gastric ulcer. In 1989, he had a transurethral prostatic resection ­ which showed myofibroadenomatous hyperplasia. At that time the patient was also treated for ischemic heart disease and chronic bronchitis.

In 1982, a well-differentiated papillary transitional cell carcinoma of the urinary bladder was diagnosed. The carcinoma was repeatedly treated by endoscopic transurethral electroresection, the last time being in 1995. In spite of local recurrences, neither metastases, nor local tumors expansion could be detected. Screening chest X-rays and ultrasound examinations of the liver, spleen, kidneys and abdominal lymph nodes were negative.

In June 1996, the patient was referred to the department of dermatology for two tumors in the left clavicular region. They were sharply demarcated, dark red tumors measuring 3 and 2 cm in diameter and protruding 2 cm above the surrounding skin. The patient reported a history of rapid growth and intermittent spontaneous bleeding (Fig. 1). Thorough examination of the patient revealed 16 additional skin lesions in the form of dark red macules and papules, 2-3 mm in diameter, situated on the left side of the chest (Fig. 2).

Histological examination of three excisions (tumor, papular and macular lesions) showed an intact epidermis and massive dermal and subcutaneous infiltration by a poorly differentiated carcinoma. The infiltrates were organized into nests and large complexes, without organoid patterns. The histocytological appearance of the tumor cells corresponded to a small-cell carcinoma of the "intermediate" type. Immunohistochemically, the tumor cells showed dot-like paranuclear positivity for cytokeratin filaments (using KL-1 antibody, Immunotech and AE1/AE3 antibody, BioGenex) and cytoplasmic NSE positivity (Dakopatts). Stainings for chromogranin A (BioGenex) and carcinoembryonal antigen (BioGenex) were negative. These findings were consistent with cutaneous metastatic involvement by a small cell carcinoma with neuroendocrine differentiation, most likely originating in the lung (Fig. 3).

Subsequent chest X-rays and CT investigations revealed multiple lung, pleural and costal metastases. Further investigations, such as bronchoscopy with lavage, or biopsy from extracutaneous masses were refused by the patient, because of his poor general health. Rapid progression of the small-cell carcinoma followed, with great numbers of new metastases to the skin of the chest, abdominal region and both arms, as well as occipital and parietal regions of the scalp with the development of alopecia neoplastica. The patient died six months after the first appearance of cutaneous metastases. Permission for autopsy was refused.

Discussion

Cutaneous metastases tend to appear first near the primary tumor [3]. Thus the common sites of cutaneous metastases are the chest, back, abdomen, scalp and neck, while occurence on the upper and lower extremities is rare [2, 3]. Cutaneous metastases portend a poor prognosis. Patients with carcinoma of the lung generally die 3-5 months after the first appearance of cutaneous metastases [2], and a similar poor prognosis is evident in patients with cutaneous metastases from other types of tumors [4].

In the present case, the patient had a history of reccurrent transitional cell carcinoma of the urinary bladder. Thus, the multiple cutaneous metastases at the time of presentation, were considered to be metastatic transitional cell carcinoma. The histological appearance of the cutaneous lesions however, was unlike papillary transitional cell carcinoma and instead showed a small cell carcinoma. The differential diagnoses of small-cell carcinoma include small-cell carcinoma metastatic from the lung, oesophagus, or gut, as well as medullary carcinoma of the thyroid, lymphoma, Merkel cell tumor and melanoma [4]. The absence of typical cytological findings of Merkel cell carcinoma, including the lack of finely dispersed "lymphoblastoma like" chromatin, caused us to favor a cutaneous metastasis [6, 7]. The origin of the tumor appears to be the lung, as the CT scan showed multiple pulmonary lesions, pleural and costal metastases.

Transitional cell carcinoma is rarely metastatic to the skin. The knowledge of the relative tendency of two different tumors to metastasize, as well as the location to where they tend to metastasize can lead the clinician to the likely diagnosis.

REFERENCES

1. Terashima T, Kanazawa M. Lung cancer with skin metastasis. Chest 1994; 106: 1448-50.

2. Coslett LM, Katlic MR. Lung cancer with skin metastasis. Chest 1990; 97: 757-9.

3. Brownstein MH, Helwig EB. Patterns of cutaneous metastasis. Arch Dermatol 1972; 105: 862-8.

4. Schwartz RA. Histopathological aspect of cutaneous metastatic disease. J Am Acad Dermatol 1995; 33: 649-57.

5. Lookingbill DP, Spangler N, Sexton FM. Skin involvement as the presenting sign of internal carcinoma. J Am Acad Dermatol 1990; 22: 19-26.

6. Eusebi V, Capella C, Cossu A, Rosai J. Neuroendocrine carcinoma within lymph nodes in the absence of a primary tumor, with special reference to Merkel cell carcinoma. Am J Surg Pathol 1992; 16: 658-66.

7. Tucci MG, Giangiacomi M, Cataldi I, Tappa MM, Rezai B, Ricotti G. Merkel cell tumor. Update on histological features and management. Skin Cancer 1996; 11: 145-53.


 

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