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Biomedical subjects

D M Go

Publications and source records attributed to D M Go.

6 recordsLinked to original sources

Primary B-cell malignant lymphoma of the maxilla with a sarcomatous pattern and multilobated nuclei.

Three cases of primary malignant lymphoma of the maxilla are reported. The primary intraosseous origin of these tumors was demonstrated by x-ray examination and surgical exploration. The initial interpretation as odontogenic infection led to a delay in starting therapy of 9 months in one case. Biopsies of two cases were initially interpreted as sarcoma because of a dense reactive fibrosis between the tumor cells. Subsequently, hemimaxillectomy was performed in one case. Histologically and ultrastructurally the tumor cells showed marked nuclear abnormalities with cleavage, folding, and lobulation. Immunohistochemical studies of two cases showed a monoclonal immunoglobulin expression, IgG-K; T-lymphocyte-associated antigens were not detected on the tumor cells. The findings indicate the existence of a primary B-cell malignant lymphoma of bone with multilobated nuclei. The lymphoid nature may be masked by a dense proliferation of connective tissue. The relation of these tumors to the classifications for malignant lymphoma of lymph node is discussed.

Adult

Primary cutaneous lymphoplasmacytoid lymphoma (immunocytoma).

A case of localized lymphoplasmacytoid lymphoma of the skin was studied by light and electron microscopy, by immunological methods, and by enzyme cytochemistry. It illustrated usual and unusual features of a type of B-cell lymphoma in the skin and presented problems in differential diagnosis. Histologically, its cellularity varied from a monomorphous to a pleomorphic pattern that was highly suggestive of a nonspecific inflammatory reaction or a pseudolymphoma, but from the presence of a clone of IgG (lambda)-producing plasmacytoid cells, it was established that it consisted in fact of lymphoplasmacytoid and polymorphic subtypes of an immunocytomatous lymphoma.

Adult

Screening errors in cervical cytologic screening.

A total of 555 cervical smears, originally classified as Papanicolaou classes I and II, from women in whom three years later cytologic findings consistent with moderate dysplasia, severe dysplasia, carcinoma in situ and invasive cancer were diagnosed were reviewed in order to estimate the screening error. The initial diagnosis proved to be underestimated in 17.5% of the smears. The two diagnoses correlated in 70.2% of the smears while 12.3% of the smears that contained no abnormality were judged to be inadequate for making a diagnosis, probably representing sampling errors. Quality-control measures to reduce these errors are briefly summarized.

Adult