Nerve biopsy findings in different patterns of proximal diabetic neuropathy

Gérard Saïd, Catherine Goulon‐Goeau, Catherine Lacroix, Antoine Moulonguet

Annals of Neurology · 1994 · 264 citations · 29 references

Concepts

TL;DR

Diabetic patients can develop focal or multifocal neuropathies, including painful proximal neuropathy of the lower limbs, but the underlying pathophysiology remains unclear. We examined 10 non‑insulin‑dependent diabetics aged 45–72 with painful proximal neuropathy, excluding other causes, and performed light and electron microscopy on biopsied intermediate cutaneous nerves of the thigh. All patients had asymmetrical proximal neuropathy (sensory in 4, motor‑sensory in the rest) with signs of distal symmetrical sensory polyneuropathy; ischemic lesions with vasculitis/inflammation were found in 3 patients, while the remaining showed axonal and demyelinating changes similar to DSSP, indicating that mild proximal neuropathy mirrors DSSP lesions, whereas severe forms involve ischemia and inflammation.

Abstract

Abstract Besides distal symmetrical sensory polyneuropathy (DSSP), middle‐aged diabetic patients may present with focal or multifocal neuropathies, including proximal neuropathy of the lower limbs, the pathophysiological features of which are uncertain. We studied 10 non–insulin‐dependent diabetic patients, 45 to 72 years of age, who developed a painful proximal neuropathy of the lower limbs for which other causes of neuropathy were carefully excluded. The proximal neuropathy was asymmetrical in all patients, sensory in 4, motor and sensory in the others. Signs of DSSP were present in all. A sample of the intermediate cutaneous nerve of the thigh, a sensory branch of the femoral nerve, was taken by biopsy and examined by light and electron microscopy. Examination of the nerve specimens revealed ischemic nerve lesions in 3 patients. Nerve ischemia was associated with vasculitis and inflammatory infiltration in 2 of them. In the other patients the lesions of the cutaneous nerve of the thigh included a varying incidence of axonal and demyelinative lesions similar to those observed in DSSP, with mild inflammatory infiltration in 4 of them. The density of myelinated and of unmyelinated was variably decreased. This study shows that axonal and demyelinative lesions similar to those found in diabetic DSSP are present in proximal nerves in mild forms of proximal diabetic neuropathy; while nerve ischemia, inflammatory infiltration, and vasculitis are encountered in the most severe forms of proximal diabetic neuropathy.

References

29