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Interdigitating dendritic reticulum cell sarcoma: cytologic, histologic and immunocytochemical features.
Gita Jayaram1, Kein Seong Mun, Elnazir Mohamed Elsayed
1Department of Pathology, University Malaya Medical Centre, Kuala Lumpur, Malaysia. gitajayaram@yahoo.com
Diagnostic Cytopathology
|June 10, 2005
Summary
This case study details a rare dendritic reticulum cell tumor, specifically interdigitating dendritic reticulum cell sarcoma. Diagnosis was confirmed through combined cytologic, histologic, and immunohistologic analysis of a cervical mass.
Area of Science:
- Oncology
- Cytopathology
- Surgical Pathology
Background:
- Dendritic reticulum cell tumors are rare neoplasms with significant morphologic overlap with other malignancies.
- The fine-needle aspiration (FNA) cytologic features of these tumors are not well-established.
- Accurate diagnosis is crucial due to potential confusion with other cancers.
Observation:
- A 33-year-old woman presented with a rapidly growing right upper cervical mass and right-sided ptosis.
- FNA cytology revealed large, polygonal cells with high nuclear-cytoplasmic ratio, irregular nuclei, prominent nucleoli, and numerous mitoses.
- Immunocytochemistry showed focal CD45 and CD68 reactivity, with negativity for B-cell and T-cell markers, CD30, EMA, and cytokeratin.
Findings:
- Histologic examination of the biopsy demonstrated nodal effacement by pleomorphic neoplastic cells, some resembling Reed-Sternberg cells, with an infiltrate of small lymphocytes.
- Immunohistochemistry confirmed tumor cell expression of vimentin, S-100 protein, CD68, and MAC387.
- The tumor cells were negative for a broad panel of markers including lymphoid, histiocytic, and epithelial markers, supporting a histiocytic/dendritic lineage.
Implications:
- The study establishes the diagnostic utility of FNA cytology combined with immunocytochemistry for rare dendritic reticulum cell tumors.
- The findings aid in differentiating interdigitating dendritic reticulum cell sarcoma from other cervical malignancies.
- This case highlights the importance of comprehensive diagnostic workup for rare neoplasms presenting with overlapping features.