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19. Phillipson OT, Bird ED. Plasma growth hormone concentrations in Huntington’s
chorea. Clin Sci Mol Med 1976;50:551e4.
20. Grottoli S, Gasco V, Ragazzoni F, et al. Hormonal diagnosis of GH hypersecretory
states. J Endocrinol Invest 2003;26:27e35.
21. Botfield C, Ross RJ, Hinds CJ. The role of IGFs in catabolism. Baillieres Clin
Endocrinol Metab 1997;11:679e97.
22. Hawker FH, Stewart PM, Baxter RC, et al. Relationship of somatomedin-C/insulin-
like growth factor I levels to conventional nutritional indices in critically ill patients.
Crit Care Med 1987;15:732e6.
23. Politis M, Pavese N, Yen F Tai, et al. Hypothalamic involvement in
Huntington’s disease: an in vivo PET study. Brain
2008;131:2860e9.
Neurological picture
Pott’s puffy tumour: harbinger of
intracranial sepsis
A 60-year-old woman presented with a 4-week history of unilat-
eral forehead swelling following a coryzal episode. She described
frontomaxillary pain and nasal discharge. Examination confirmed
afluctuant non-tender swelling (figure 1A) and ipsilateral muco-
purulent rhinorrhoea. Neuro-ophthalmic examinations were
unremarkable. A contrast-enhanced CTscan revealed a right-sided
pansinusitis (figure 1B), an external subperiosteal collection with
an underlying small extradural collection (figure 1C) and an
interposed rarefied frontal bone (figure 1D). She underwent
endoscopic sinus drainage with external frontal sinus trephine.
The intracranial collection was managed conservatively with
intravenous antibiotics and serial CT scans.
COMMENT
Pott’s puffy tumour describes a subperiosteal abscess overlying
frontal bone osteomyelitis. First documented as a sign of intra-
cranial empyema following head injury (1768) and subsequently
as a complication of frontal sinusitis (1775),
1
fewer than 20
adult cases have been reported in the post-antibiotic era.
2
It has
Figure 1 (A) Clinical photograph of
unilateral forehead swelling. Coronal CT
scans demonstrate (B) opacification of
the right maxillary and ethmoid sinuses
and nasofrontal duct. Axial CT images
demonstrate (C) an extracranial
subperiosteal collection and underlying
extradural empyema with (D)
rarefaction of the interposed frontal
bone.
J Neurol Neurosurg Psychiatry May 2011 Vol 82 No 5 547
Research paper
group.bmj.com on June 30, 2012 - Published by jnnp.bmj.comDownloaded from
also occurred as a late complication of neurosurgery,
3
cocaine
abuse
4
and dental sepsis.
5
Both Pott’s puffy tumour and its associated complications are
facilitated by the system of valveless veins draining the frontal
sinus mucosa, which promote septic emboli to seed the adjacent
bone, dura and cerebral parenchyma. Extension may also occur
via natural foramina or direct bone erosion. Intracranial
complications have been reported to occur in as many as 85% of
cases
6
and include meningitis, epidural or subdural empyema,
frontal lobe abscess and cavernous sinus thrombosis in addition
to orbital infections.
7
While the typical presentation is that of forehead swelling
with headache and fever, patients are frequently systemically
well and often without a clear history of preceding sinusitis.
8
Diagnostic imaging involves a combination of contrast-
enhanced CT of the head and paranasal sinuses and MRI with
gadolinium enhancement to exclude intracranial complications.
9
Gallium-67 scintigraphy has been employed to aid delineation of
osteomyelitic bone.
10
Causative organisms reflect those seen in chronic rhinosi-
nusitis wherein protracted mucosal oedema obstructs sinus
ostia and fosters a polymicrobial microaerophilic and anaer-
obic growth.
11 12
Isolated species have included Streptococci,
Staphylococci,Haemophilus influenzae,Enterococci and Bacteroides
spp.
13
Treatment involves a combination of surgical and medical
therapy. Surgical goals are abscess drainage, debridement of
osteomyelitic sequestra and obtaining tissue for Gram stain and
culture. Simultaneous external or endoscopic drainage of the
involved paranasal sinus is advised
14
with a breach of the
posterior table of the frontal sinus best managed by its cranial-
isation.
15
While bicoronal scalp flaps may provide optimum
surgical access, some have achieved clearance through eyebrow
incisions
16
and occasionally through serial aspiration.
17
If
craniotomy is performed, care must be taken to avoid damage to
the adherent dura under the diseased calvarium as perforation
may seed infection into the subarachnoid space.
14
A review of contemporary cases supports the early empirical
administration of broad spectrum antibiotics with anaerobic and
methicillin-resistant Staphylococcus aureus cover and good CNS
penetration prior to culture-directed therapy.
18
An appropriate
combination is ceftriaxone, metronidazole and vancomycin, but
consultation with local microbiologists is advised.
19
The
minimum duration of therapy may be 6 weeks and it may be
continued depending upon clinical response.
2
Close clinical and
radiological follow-up is required to allow the early identification
and treatment of recrudescent disease.
Yogesh M Bhatt, Antonio Belloso
Department of Otorhinolaryngology Head and Neck Surgery, Royal Blackburn Hospital,
Blackburn, Lancashire, UK
Correspondence to Mr Yogesh M Bhatt, Specialist Registrar in Otolaryngology,
Head-Neck Surgery, Department of Otorhinolaryngology Head and Neck Surgery,
Royal Blackburn Hospital, Haslingden Road, Blackburn, Lancashire BB2 3HH, UK;
bhatt_ym@yahoo.co.uk
Competing interests None.
Patient consent Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.
Accepted 14 January 2011
Published Online First 9 February 2011
J Neurol Neurosurg Psychiatry 2011;82:547e548. doi:10.1136/jnnp.2010.239327
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adults: a report of 4 frontal bone infections and a review of the literature. Scand J
Infect Dis 2001;33:263e5.
4. Noskin GA, Kalish SB. Pott’s puffy tumor: a complication of intranasal cocaine
abuse. Rev Infect Dis 1991;13:606e8.
5. Chandy B, Todd J, Stucker FJ, et al. Pott’s puffy tumor and epidural abscess arising
from dental sepsis: a case report. Laryngoscope 2001;111:1732e4.
6. Singh B, Van Dellen J, Ramjettan S, et al. Sinogenic intracranial complications.
J Laryngol Otol 1995;109:945e50.
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this unforgotten entity. Case report and review of the literature. J Neurosurg
2006;105(2 Suppl):143e9.
8. Forgie SE, Marrie TJ. Pott’s puffy tumor. Am J Med 2008;121:1041e2.
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10. Wells RG, Sty JR, Landers AD. Radiological evaluation of Pott puffy tumor. JAMA
1986;255:1331e3.
11. Verbon A, Husni RN, Gordon SM, et al. Pott’s puffy tumor due to Haemophilus
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2002;8:381e2.
13. Bambakidis NC, Cohen AR. Intracranial complications of frontal sinusitis in children:
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J Neurosurg 1996;84:110e12.
15. Minutilli E, Pompucci A, Anile C, et al. Cutaneous fistula is a rare presentation of
Pott’s puffy tumour. J Plast Reconstr Aesthet Surg 2008;61:1246e8.
16. Karaman E, Hacizade Y, Isildak H, et al. Pott’s puffy tumor. J Craniofac Surg
2008;19:1694e7.
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computed tomography findings. J Craniofac Surg 2008;19:1697e9.
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from pansinusitis. J Emerg Med Published Online First: 18 Nov 2008.
doi:10.1016/j.jemermed.2008.04.050.
19. Guille
´nA,Brell M, Cardona E, et al. Pott’s puffy tumour: still not an eradicated
entity. Childs Nerv Syst 2001;17:359e62.
548 J Neurol Neurosurg Psychiatry May 2011 Vol 82 No 5
Neurological picture
group.bmj.com on June 30, 2012 - Published by jnnp.bmj.comDownloaded from
doi: 10.1136/jnnp.2010.239327
online February 9, 2011 2011 82: 547-548 originally publishedJ Neurol Neurosurg Psychiatry
Yogesh M Bhatt and Antonio Belloso
intracranial sepsis
Pott's puffy tumour: harbinger of
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