Intranodal palisaded myofibroblastoma
| Intranodal palisaded myofibroblastoma | |
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| Classification and external resources | |
 Micrograph of an intranodal palisaded myofibroblastoma. H&E stain. |
Intranodal palisaded myofibroblastoma, abbreviated IPM, is a rare primary tumour of lymph nodes, that classically presents as an inguinal mass.[1]
It afflicts predominantly males of middle age.
Signs and symptoms
IPMs present as painless lymphadenopathy.[1] They usually are found in the inguinal region and grow slowly.
The signs and symptoms are non-specific, i.e. it is not possible to diagnose an IPM from the symptoms and manner in which they present.
The main (clinical) differential diagnosis of IPM is metastatic cancer, e.g. squamous cell carcinoma, malignant melanoma, adenocarcinoma.
Diagnosis
IPMs are diagnosed by examination of the tissue by a pathologist.
They have a rim of peripheral lymphoid tissue (remnant of a lymph node) and consist of spindle cells with nuclear palisading. Red blood cell extravasation is common and blood vessels surrounded by collagen with (fine) peripheral spokes (amianthoid fibers) are usually seen.[2]
Immunostains for smooth muscle actin and cyclin D1 are characteristically positive. The main histologic differential diagnosis is schwannoma.
Treatment
Simple surgical excision is considered curative. Rare recurrences have been reported.[3]
See also
Additional images
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References
- ↑ 1.0 1.1 Nguyen, T.; Eltorky, MA. (Feb 2007). "Intranodal palisaded myofibroblastoma.". Arch Pathol Lab Med 131 (2): 306–10. doi:10.1043/1543-2165(2007)131[306:IPM]2.0.CO;2. PMID 17284119.
- ↑ Bigotti, G.; Coli, A.; Mottolese, M.; Di Filippo, F. (Sep 1991). "Selective location of palisaded myofibroblastoma with amianthoid fibres.". J Clin Pathol 44 (9): 761–4. PMC 496726. PMID 1918406.
- ↑ Creager, AJ.; Garwacki, CP. (May 1999). "Recurrent intranodal palisaded myofibroblastoma with metaplastic bone formation.". Arch Pathol Lab Med 123 (5): 433–6. doi:10.1043/0003-9985(1999)1230433:RIPMWM2.0.CO;2. PMID 10235504.
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