Fusiform incisional biopsy for pigmented skin lesions.

Current recommendations for biopsy of a pigmented skin lesion suspected of being melanoma include complete excision when possible. Because benign pigmented lesions do not warrant excisional biopsy, especially when they are large and/or on cosmetically sensitive sites, incisional biopsy is desirable. For such lesions we recommend a fusiform incisional biopsy. This tissue sampling technique not only yields an excellent cosmetic outcome, but also provides the pathologist with an optimal biopsy specimen in which he/she can assess the symmetry, circumscription, breadth, and depth of the lesion.

Cytomorphologic features of Merkel cell carcinoma in fine needle aspiration biopsies. A study of two atypical cases.

OBJECTIVE: To report atypical cytomorphologic features in fine needle aspiration biopsies (FNABs) from two cases of Merkel cell carcinoma (MCC), a primary neuroendocrine neoplasm of skin. STUDY DESIGN: Retrospective review of FNABs with histologic correlation from six patients with MCC and a report of findings from two whose smears showed atypical features. RESULTS: Typically the aspirates produce highly cellular smears of loosely clustered and individual, relatively monomorphic, small tumor cells with round to oval, regularly contoured nuclei. In two of our cases, the tumor cell nuclei exhibited a spectrum of pleomorphism ranging from moderately complex nuclear membranes with cleaves, indentations and protrusions in one case to large, markedly bizarre, convoluted nuclei and multinucleate tumor cells in the extreme case. Both cases were primary neoplasms, and the diagnosis was based on clinical, histologic and immunohistochemical data. Additionally, electron microscopy was performed on the tumor with bizarre nuclei and demonstrated rare, dense core neurosecretory granules and paranuclear bundles of intermediate filaments.

Leiomyosarcoma of the esophagus: radiographic findings in 10 patients.

OBJECTIVE: Leiomyosarcomas of the esophagus are rare malignant smooth-muscle tumors that have been described only anecdotally in the radiology literature. The objective of this study was to evaluate the clinical and radiographic findings of this unusual lesion. MATERIALS AND METHODS: A search of the radiology archives of the Armed Forces Institute of Pathology revealed 10 cases of esophageal leiomyosarcomas. Clinical and radiographic findings were reviewed retrospectively. RESULTS: All but one patient presented with dysphagia. The average duration of the dysphagia was 6.7 months, but five patients had dysphagia for 3 or fewer months. Frontal chest radiographs revealed a mediastinal mass in five patients. Barium studies revealed intramural lesions in six patients, intraluminal lesions in two, and infiltrative lesions in two. The intramural Lesions all had large exophytic components, and three contained ulceration or tracking. One of the intraluminal lesions appeared as a polypoid expansile mass and the other, as a smooth expansile sausage-shaped mass mimicking a fibrovascular polyp. CT revealed a mass involving the esophagus in five patients; three of these patients had heterogeneous lesions containing large exophytic components, central areas of low density, and extraluminal gas or contrast material within the tumor. In two patients, MR imaging revealed large masses that were isointense with skeletal muscle on T1-weighted images and hyperintense on T2-weighted images. CONCLUSION: Our experience suggests that esophageal leiomyosarcomas have radiographic findings similar to those of leiomyosarcomas elsewhere in the gastrointestinal tract. Esophageal leiomyosarcomas have a better prognosis than squamous cell carcinomas and are often amenable to surgical cure.

Fibrovascular polyps of the esophagus: clinical, radiographic, and pathologic findings in 16 patients.

OBJECTIVE: Fibrovascular polyps of the esophagus are rare benign nonneoplastic intraluminal masses. Most published reports of patients with these polyps have been anecdotal. The purpose of this study was to reassess the clinical, radiographic, and pathologic findings in a relatively large series of patients with this unusual tumorlike lesion. MATERIALS AND METHODS: A search of the radiologic archives of the Armed Forces Institute of Pathology revealed 16 cases of fibrovascular polyps of the esophagus. We reviewed the clinical, radiographic, and pathologic findings in these 16 cases. RESULTS: All 16 patients were symptomatic. Fourteen (87%) had dysphagia and four (25%) had respiratory symptoms. The average duration of symptoms was 17 months, but seven patients (44%) had symptoms for 6 or fewer months. Two patients (12%) had a history of regurgitating the tumor into the pharynx or mouth, but none had the known complication of asphyxiation due to occlusion of the larynx. Chest radiographs revealed a right-sided superior mediastinal mass and/or anterior tracheal bowing in seven patients (44%). Barium studies revealed smooth but variably lobulated intraluminal masses that originated in the lower cervical esophagus and had variable sizes and distal extents, with an average length of 15 cm. Depending on the amount of fat and fibrovascular tissue in the lesion, CT revealed a heterogeneous appearance in four patients, lesions of predominantly fat density in two, and lesions of predominantly soft-tissue density in two. CONCLUSION: Knowledge of the clinical and radiographic features of fibrovascular polyps of the esophagus is important because surgical removal of these lesions is warranted in most patients.

Cytology of fluids from pleural, peritoneal and pericardial cavities in children. A comprehensive survey.

We reviewed all cytologic specimens of pleural, peritoneal and pericardial fluids examined in our laboratory from patients aged 0-17 years during a 12-year period. A total of 103 specimens were studied: 45 pleural, 54 peritoneal and 4 pericardial. Twenty-two of the 103 specimens were peritoneal washes. Eleven of the 81 (14%) serous effusion specimens contained tumor cells: 8 lymphomas, 1 leukemia, 1 abdominal desmoplastic small round cell tumor and 1 Wilms' tumor. Two false-positive diagnoses were made in patients presenting with ascites with an unknown case. Both cases were complicated by the presence of atypical mononuclear cells and illustrate a potential pitfall in the evaluation of pediatric serous effusions. We conclude: (1) Almost all pediatric effusions are benign. (2) Malignant pediatric effusions are usually caused by neoplasms of the small cell type, mostly lymphoreticular. (3) The major diagnostic difficulty in interpreting pediatric effusion cytology is in distinguishing neoplasms of the small cell type from mononuclear inflammatory cells. (4) The usefulness of peritoneal washings in pediatric patients is similar to that in adults.