Intranodal palisaded myofibroblastoma

Intranodal palisaded myofibroblastoma
Micrograph of an intranodal palisaded myofibroblastoma. H&E stain.
Specialty	Oncology

Intranodal palisaded myofibroblastoma (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.^{[citation needed]} The main (clinical) differential diagnosis of IPM is metastatic cancer, e.g. squamous cell carcinoma, malignant melanoma, adenocarcinoma.^{[citation needed]}

Diagnosis

IPMs are diagnosed by examination of the tissue by a pathologist.^{[citation needed]} 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.^{[citation needed]}

• 
  Low mag.
• 
  High mag.

Treatment

Simple surgical excision is considered curative. Rare recurrences have been reported.^[3]

See also

• Schwannoma

References

This page was last edited on 30 April 2024, at 09:18