New insights into the development of popliteal cysts.

BACKGROUND: This prospective study was designed to investigate the aetiology of popliteal (Baker's) cysts. METHODS: Some 426 legs in 312 individuals were investigated with ultrasonography for the presence of a popliteal cyst. Participants included healthy volunteers, patients with a painful knee, and a group of patients with signs and symptoms of deep vein thrombosis (DVT). The location, thickness and content of all cysts were recorded. In addition, the popliteal fossa was dissected in four cadaver knees. RESULTS: The prevalence of popliteal cyst increased with age and was significantly higher in those aged over 50 years (P < 0.001). Compared with controls (incidence 3.0 per cent), cysts were more common in patients with DVT symptoms (9.5 per cent; P = 0.141) and those with painful knees (19.8 per cent; P < 0.001). All cysts were located in the posteromedial aspect of the popliteal fossa; the majority extended between the deep fascia and the medial head of the gastrocnemius muscle. At this level an area without external support of the posterior capsule was identified between the two expansions of the semimembranosus muscle from the medial side (the oblique popliteal ligament and the expansion over the popliteus muscle) and the posterior cruciate ligament from the lateral side. This area was also located in the knee dissections. No association was found between popliteal cyst and acute DVT. CONCLUSION: Popliteal cysts are relatively common in patients over 50 years old with a painful knee or with signs and symptoms of DVT. They form in the posteromedial popliteal fossa because the synovial capsule does not provide anatomical support in this region.

Neuroprotective utility and neurotrophic action of neurturin in postnatal motor neurons: comparison with GDNF and persephin.

Neurturin and persephin are recently discovered homologs of glial cell line-derived neurotrophic factor (GDNF). Here, we report that neurturin, like GDNF, increases the choline acetyltransferase activity of normal postnatal motor neurons, induces neurite outgrowth in spinal cord, and potently protects motor neurons from chronic glutamate-mediated degeneration. Persephin, in contrast, does not appear to have neurotrophic or neurite-promoting effects on mature motor neurons and may instead worsen the glutamate injury of motor neurons. This pattern in the TGF-beta family suggests certain receptor specificities, requiring at least the Ret/GFRalpha-1 receptor complex. The results predict potential benefit of neurturin, but not persephin, in the treatment of motor neuron disorders and spinal cord diseases.