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Anna Pichiecchio, Carla Uggetti, Maria Grazia Egitto, and Federico Zappoli
ParryRomberg syndrome with migraine and intracranial aneurysm
Neurology 2002; 59: 606-608
[Abstract][Full text][PDF]
anna.pichiecchio{at}mondino.it Anna Pichiecchio, et al.
We thank Dr. Olivares-Romero for his interest in our article. We note
he previously described a further case of Parry – Romberg syndrome whose
clinical and MR findings could further support the malformative
hypothesis, initially proposed by Dupont and Schievink [2, 5] and further
supported by our patients’ findings. The possibility that the disease
could be related to a damage of the neural plate during its early
development now seems likely; further careful clinical examinations and
genetic researches need to be done to add more to our understanding of
the complex pathogenetic mechanisms underlying Progressive Facial
Hemiatrophy.
5. Schievink WI, Mellinger JF, Atkinson JLD. Progressive intracranial
aneurysmal disease in a child with progressive hemifacial atrophy (Parry-
Romberg disease): case report. Neurosurgery 1996;38:1237-1240.
Parry–Romberg syndrome with migraine and intracranial aneurysm
3 October 2002
Jesús Olivares-Romero, Neurologist. Neurology Service. Hospital Torrecárdenas. ALMERÍA. SPAIN., PJ Serrano-Castro, JI Peralta-Labrador, P Guardado-Santervás, A. Arjona-Padillo and E. Goberna-Ortiz
pserrano{at}meditex.es Jesús Olivares-Romero, et al.
We read with interest the article of Pichiecchio et al [1] of a new case of Progressive Facial Hemiatrophy (PFH) associated
with migraine and intracranial aneurysm. The authors suggest a
malformative hypothesis with involvement, at the same time, of vascular
and mesenchymal structures with common progenitors in the neural crest.
This hypothesis had been previously suggested [2-4].
We recently published a case of PFH followed up
for 13 years [4]. During this time, the patient associated
clinical signs of progressive cortical (with partial clonic seizures in the
right leg with jacksonian progression and secondary generalization) and
cerebellar dysfunction (dysartrhia and ataxia). The MRI showed a pattern of progressive atrophy of left temporal,
pontine, mesencephalic and cerebellar structures. These structures are
embryologically related to ipsilateral rostral neural tube. This supports the hypothesis that damage occured during the early development of the neural
plate.
REFERENCES
1) Pichiecchio A, Uggetti C, Egitto MG, Zappoli F. Parry-Romberg
syndrome with migraine and intracranial aneurysm. Neurology 2002; 59: 606-
608.
2) Dupont S, Catala M, Hasboun D, et al. Progressive facial
hemiatrophy and epilepsy: a common underlying dysgenetic mechanism.
Neurology 1997; 48: 1013-18
3) Derex L, Isnard H, Revol M. Progressive facial hemiatrophy with
multiple benign tumors and hamartomas. Neuropediatrics 1995; 26: 306-9.
4) Olivares -Romero J, Casado -Torres A, Serrano- Castro PJ, et al.
Hemiatrofia facial progresiva de Parry-Romberg: consideraciones
patogénicas y evolutivas a propósito de un caso con seguimiento
prolongado. Rev Neurol 1999; 29: 1032-1035.