Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-23T14:28:24.323Z Has data issue: false hasContentIssue false
  • English
  • Français

Large, solitary angiokeratoma in the posterior third and base of the tongue: case report

Published online by Cambridge University Press:  21 June 2011

M Dutta ,
S Ghatak ,
G Biswas  and
R Sinha
M Dutta
Affiliation:
Department of Otorhinolaryngology and Head Neck Surgery, R G Kar Medical College and Hospital, Kolkata, West Bengal, India
S Ghatak
Affiliation:
Department of Otorhinolaryngology and Head Neck Surgery, R G Kar Medical College and Hospital, Kolkata, West Bengal, India
G Biswas
Affiliation:
Department of Otorhinolaryngology and Head Neck Surgery, R G Kar Medical College and Hospital, Kolkata, West Bengal, India
R Sinha*
Affiliation:
Department of Otorhinolaryngology and Head Neck Surgery, R G Kar Medical College and Hospital, Kolkata, West Bengal, India
*
Address for correspondence: Dr (Prof) Ramanuj Sinha, 4RA, 2/1, Purbachal, Salt Lake, Kolkata 700097, West Bengal, India Fax: +91 33 28281551 E-mail: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

Objective:

We present an extremely rare case of isolated angiokeratoma of the tongue.

Method:

Case report and review of related literature.

Results:

An 18-year-old, male adolescent presented with a fleshy, intermittently bleeding mass in the posterior third and base of the tongue. The lesion was initially suspected to be a lingual thyroid or haemangioma, but histopathological features were consistent with angiokeratoma. Magnetic resonance imaging revealed that the lesion extended up to the vallecula and involved the lamina propria and superficial tongue musculature. No similar lesions were found elsewhere in the body. No metabolic derangements were identified in the patient or his family. The 2.6 × 1.5 × 0.5 cm mass was excised under general anaesthesia.

Conclusion:

We present the 1st case of isolated lingual angiokeratoma in a male, the 4th such case overally, the largest ever documented. The lesion was situated in the posterior third and base of the tongue, a position not previously described.

Keywords

AngiokeratomaOral CavityTongue
Type
Clinical Records
Information
The Journal of Laryngology & Otology , Volume 125 , Issue 10 , October 2011 , pp. 1083 - 1086
Copyright
Copyright © JLO (1984) Limited 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1Sion-Vardy, N, Manor, E, Puterman, M, Bodner, L. Solitary angiokeratoma of the tongue. Med Oral Pathol Oral Cir Bucal 2008;13:E12–4Google ScholarPubMed
2Leung, CS, Jordan, RCK. Solitary angiokeratoma of the oral cavity. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1997;84:51–3CrossRefGoogle ScholarPubMed
3Siponem, M, Penna, T, Apaja-Sarkkinem, M, Palatsi, R, Salo, T. Solitary angiokeratoma of the tongue. J Oral Pathol Med 2006;35:252–3CrossRefGoogle Scholar
4Ergun, S, Mete, Ö, Yeşel, S, Tanyeri, H. Solitary angiokeratoma of the tongue treated with diode laser. Lasers Med Sci 2009;24:123–5CrossRefGoogle ScholarPubMed
5Bhargava, P, Bhargava, S, Mathur, D, Agarwal, DS, Bhargava, R. Angiokeratoma of tongue. Indian J Dermatol Venereol Leprol 2001;67:270Google ScholarPubMed
6Mibelli, V. A new form of de-keratosis, angiokeratoma [in Italian]. G Ital Mal Vener 1891;30:285Google Scholar
7Imperial, R, Helwig, EB. Angiokeratoma. Arch Dermatol 1967;95:166–75CrossRefGoogle ScholarPubMed
8Fernandez-Flores, A, Sanroman, J. Solitary angiokeratoma of the tonsillar pillar of the oral cavity. Rom J Morphol Embryol 2009;50:115–17Google ScholarPubMed
9Nausheen, Y, Aamir, A, Zubair, A, Akhter, H, Rashid, A, Naila, K et al. Angiokeratoma of tongue – a series of 14 cases. J Pak Med Assoc 2006;56:285–7Google Scholar
10Schiller, PI, Itin, PH. Angiokeratomas: an update. Dermatology 1996;193:275–82CrossRefGoogle ScholarPubMed
11Segura-Saint-Gerons, R, Toro-Rojas, M, Ceballos-Salobreña, A, Aparicio-Soria, JL, Fuentes-Vaamonde, H. Focal epithelial hyperplasia. A rare disease in our area. Med Oral Patol Oral Cir Bucal 2005;10:128–31Google ScholarPubMed
12del Pozo, J, Fonseca, E. Angiokeratoma circumscriptum naeviforme: successful treatment with carbon-dioxide laser vaporization. Dermatol Surg 2005;2:232–6CrossRefGoogle Scholar
13Gorse, SJ, James, W, Murison, MS. Successful treatment of angiokeratoma with potassium tritanyl phosphate laser. Br J Dermatol 2004;3:620–2CrossRefGoogle Scholar