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                   Histopathology Image of

       Fibrolipomatous Hamartoma of Nerve 4

                                      

 
Reactive and hamartomatous lesions:

Traumatic neuroma

Morton's neuroma

Digital Pacinian neuroma

Nerve Sheath Ganglion

Fibrolipomatous hamartoma of nerve

Benign tumours:

Solitary circumscribed neuroma

(palisaded encapsulated neuroma)

Schwannoma (neurilemmoma)
and variants                          

Neurofibroma and variants 

Perineurioma   

Dermal nerve sheath myxoma
(neurothekeoma)

Cellular neurothekeoma

Granular cell tumour 

Malignant tumour:

Malignant peripheral nerve sheath tumour

Neuroendocrine Carcinoma:

Merkel cell (neuroendocrine) carcinoma

Malignant primitive neuroectodermal tumour   

Miscellaneous neuroectodermal tumours presenting in soft tissue

Subcutaneous Myxopapillary Ependymoma  

Heterotopic Glial Nodule

Heterotopic Meningeal Lesions

E-book - History of  Medicine with special reference to India
Myxoid Tumours of Soft Tissue

Classification of Soft Tissue Tumour

Gross examination of soft tissue specimen          

A practical approach to histopathological reporting of soft tissue tumours

Grading of soft tissue tumours

Lipomatous tumours

Neural tumours

Myogenic tumours

Vascular tumours

Fibroblastic/Myofibroblastic tumours

 Fibrolipomatous Hamartoma of Nerve

Visit:  Soft Tissue Pathology

Fibrolipomatous hamartoma of nerve. J Foot Ankle Surg. 1994 Jan-Feb;33(1):64-71.

Fibrolipomatous hamartomas of nerve are rare, benign, fibrofatty malformations of peripheral nerves, most commonly affecting the median nerve. Lower extremity cases are extremely rare. The authors present a very rare case of a fibrolipomatous hamartoma involving the superficial peroneal nerve, and review the literature regarding its clinical presentation and surgical management.


Fibrolipomatous hamartoma of nerve arising in the brachial plexus.
J Hand Surg [Br]. 1995 Feb;20(1):16-8.

Fibrolipomatous hamartoma of nerve is a rare benign infiltrating condition of peripheral nerves leading to progressive functional loss. Previous descriptions have virtually all been confined to the distal part of the upper limb, with the median nerve being the commonest reported site. Most cases occur in the first 3 decades of life and a third are associated with macrodactyly. A case is described in a 63-year-old woman, involving the whole of the brachial plexus, a previously unreported site for this particular lesion.

 

March  2008 
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