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Calculi and intracellular ochronosis in the submandibular tissues from a patient with alkaptonuria.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published

Standard

Calculi and intracellular ochronosis in the submandibular tissues from a patient with alkaptonuria. / Taylor, Adam; Wilson, Peter J. M.; Ingrams, D. R. et al.
In: Journal of Clinical Pathology, Vol. 63, No. 2, 02.2010, p. 186-188.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Taylor, A, Wilson, PJM, Ingrams, DR, Helliwell, TR, Gallagher, JA & Ranganath, LR 2010, 'Calculi and intracellular ochronosis in the submandibular tissues from a patient with alkaptonuria.', Journal of Clinical Pathology, vol. 63, no. 2, pp. 186-188. https://doi.org/10.1136/jcp.2009.071365

APA

Taylor, A., Wilson, P. J. M., Ingrams, D. R., Helliwell, T. R., Gallagher, J. A., & Ranganath, L. R. (2010). Calculi and intracellular ochronosis in the submandibular tissues from a patient with alkaptonuria. Journal of Clinical Pathology, 63(2), 186-188. https://doi.org/10.1136/jcp.2009.071365

Vancouver

Taylor A, Wilson PJM, Ingrams DR, Helliwell TR, Gallagher JA, Ranganath LR. Calculi and intracellular ochronosis in the submandibular tissues from a patient with alkaptonuria. Journal of Clinical Pathology. 2010 Feb;63(2):186-188. doi: 10.1136/jcp.2009.071365

Author

Taylor, Adam ; Wilson, Peter J. M. ; Ingrams, D. R. et al. / Calculi and intracellular ochronosis in the submandibular tissues from a patient with alkaptonuria. In: Journal of Clinical Pathology. 2010 ; Vol. 63, No. 2. pp. 186-188.

Bibtex

@article{cde79310ec1f4d13b6f6e4946f5a8493,
title = "Calculi and intracellular ochronosis in the submandibular tissues from a patient with alkaptonuria.",
abstract = "Alkaptonuria (AKU) is a rare autosomal recessive condition caused by deficiency of the enzyme homogentisate 1,2 dioxygenase, resulting in widespread deposition of oxidised homogentisic acid (HGA) polymer, primarily in joint tissues but also in other connective tissues. Macroscopic pigmentation of connective tissues in AKU is well documented and is the end point of a process that is not understood. Deposition in less common regions may provide clues to the pigment formation process. This is the first report of detection of ochronotic pigment in acinar cells and lumina in the submandibular gland of a patient with AKU. Deposition was noted in the apical region of the cells. A lobar duct presented a large calculus with unusual deposits possibly associated with calcium salts. This report highlights the effect that local and intracellular factors may have on converting HGA into polymeric derivatives in the absence of an extracellular matrix.",
author = "Adam Taylor and Wilson, {Peter J. M.} and Ingrams, {D. R.} and Helliwell, {T. R.} and Gallagher, {James A.} and Ranganath, {L. R.}",
year = "2010",
month = feb,
doi = "10.1136/jcp.2009.071365",
language = "English",
volume = "63",
pages = "186--188",
journal = "Journal of Clinical Pathology",
issn = "1472-4146",
publisher = "BMJ Publishing Group",
number = "2",

}

RIS

TY - JOUR

T1 - Calculi and intracellular ochronosis in the submandibular tissues from a patient with alkaptonuria.

AU - Taylor, Adam

AU - Wilson, Peter J. M.

AU - Ingrams, D. R.

AU - Helliwell, T. R.

AU - Gallagher, James A.

AU - Ranganath, L. R.

PY - 2010/2

Y1 - 2010/2

N2 - Alkaptonuria (AKU) is a rare autosomal recessive condition caused by deficiency of the enzyme homogentisate 1,2 dioxygenase, resulting in widespread deposition of oxidised homogentisic acid (HGA) polymer, primarily in joint tissues but also in other connective tissues. Macroscopic pigmentation of connective tissues in AKU is well documented and is the end point of a process that is not understood. Deposition in less common regions may provide clues to the pigment formation process. This is the first report of detection of ochronotic pigment in acinar cells and lumina in the submandibular gland of a patient with AKU. Deposition was noted in the apical region of the cells. A lobar duct presented a large calculus with unusual deposits possibly associated with calcium salts. This report highlights the effect that local and intracellular factors may have on converting HGA into polymeric derivatives in the absence of an extracellular matrix.

AB - Alkaptonuria (AKU) is a rare autosomal recessive condition caused by deficiency of the enzyme homogentisate 1,2 dioxygenase, resulting in widespread deposition of oxidised homogentisic acid (HGA) polymer, primarily in joint tissues but also in other connective tissues. Macroscopic pigmentation of connective tissues in AKU is well documented and is the end point of a process that is not understood. Deposition in less common regions may provide clues to the pigment formation process. This is the first report of detection of ochronotic pigment in acinar cells and lumina in the submandibular gland of a patient with AKU. Deposition was noted in the apical region of the cells. A lobar duct presented a large calculus with unusual deposits possibly associated with calcium salts. This report highlights the effect that local and intracellular factors may have on converting HGA into polymeric derivatives in the absence of an extracellular matrix.

U2 - 10.1136/jcp.2009.071365

DO - 10.1136/jcp.2009.071365

M3 - Journal article

VL - 63

SP - 186

EP - 188

JO - Journal of Clinical Pathology

JF - Journal of Clinical Pathology

SN - 1472-4146

IS - 2

ER -