The case of an 83-year-old woman with an uncommon presentation of cutaneous metastases from muscle-invasive transitional cell carcinoma of the urinary bladder is reported. The band-like eruption of the metastatic lesion can often be misdiagnosed and treated initially as herpes zoster. A detailed immunohistochemical analysis is also described to differentiate metastatic lesions from other sources. C utaneous metastasis from bladder carcinoma is rare. Of the cutaneous metastasis from genitourinary organs, transitional cell carcinoma (TCC) of the bladder accounts for 17% of cases.1 Clinical diagnosis can often be difficult owing to non-specific appearances of these lesions, which can vary from nodular to sclerodermoid skin lesions. With the availability of antibodies to different cytokeratins (CKs), it is possible to define the tissue-specific profiles of cytokeratins staining by immunohistochemistry.2 The differential expression of cytokeratins by different epithelial tissues can be used to subclassify epithelial tumours from different organs. We describe an immunohistochemical profile of a herpetiform metastatic lesion from muscleinvasive TCC of the urinary bladder. CASE REPORTAn 83-year-old woman presented with a 3-week history of gross haematuria. She underwent a transurethral resection of a solid-looking bladder tumour. The radiological investigation, which included a computed tomography scan of the abdomen, showed a large bladder tumour with perivesicle extension. The upper urinary tract was normal. Chest x ray was normal and the histopathological examination showed a poorly differentiated (pT2 G3) muscle-invasive TCC of the bladder associated with carcinoma in situ. Six weeks later, she presented with multiple reddish nodules on the left side of her neck and chest (fig 1). Biopsy of the lesion showed metastatic carcinoma, with appearance similar to TCC of the urinary bladder (fig 2, 3). Immunocytochemical analysis indicated that these cells were positive for CK7 (fig 4) and CK20 ( fig 5). An algorithm (table 1) was used to exclude metastases from most common sites in female subjects. She underwent four fractions of palliative radiotherapy to her pelvis, owing to problems with persistent bleeding and pain, and a single fraction of radiotherapy to the metastasis on her left chest wall owing to ulceration after biopsy. We found no clinical evidence of healing of the ulcer. She died at a followup of 6 months. DISCUSSIONCutaneous metastasis from primary bladder carcinoma is a rare event and carries a poor prognosis.1 The primary sites for metastatic bladder cancer are the liver, lung and bone. Our patient presented with haematuria and was diagnosed as having TCC of the bladder. Six weeks later, she developed a herpetiform rash on her neck and chest wall. Owing to the diagnostic dilemma and a suspicion of skin metastasis, a punch biopsy of the lesion was carried out, which showed a metastatic, poorly differentiated carcinoma in the dermis. Immunohistochemical analysis showed that the tumour cells were negative for...
South Africa 10 asymptomatic young male patients with moderate splenomegaly detected at a routine examination are presented. The history and clinical examination failed to reveal the aetiology of the splenomegaly. Further investigations, including screening for blood dyscrasias, clotting abnormalities and reticuloendothelial abnormalities were likewise unrevealing. Liver biopsies, rectal biopsies for bilharzia and bone marrow aspirates for Gaucher's Disease were found to be normal. Serology for malaria and Ebstein Barr Virus infection was also negative. Positive immunofluorescent tests for IgG antibodies specific for cytomegalovirus were found in 5 patients. We consider that these patients have splenomegaly which is not of a specific nature, but may be associated with a severe antigeneic response to the previous cytomegalovirus infection. In view of the otherwise negative findings these patients should be considered to have 'True Idiopathic Splenomegaly', a term which would indicate the benign nature of the splenic enlargement. This diagnosis should be considered in the differential diagnosis of asymptomatic patients who have splenomegaly of undetermined origin. % I lympho-
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