A novel, noninvasive imaging technique for intraoperative assessment of parathyroid glands: confocal reflectance microscopy.

BACKGROUND Successful surgical management of primary hyperparathyroidism requires the ability to identify and distinguish normal from abnormal parathyroid tissue. Microscopic pathologic confirmation often helps with the diagnoses and decisions regarding the extent of parathyroid resection. Confocal reflectance microscopy (CRM) is an optical method of noninvasively imaging tissue without fixation, sectioning, and staining as in standard histopathology. The goal of this study was to determine if CRM imaging could be used to distinguish normal from diseased parathyroid tissue intraoperatively. METHODS In this study, 44 parathyroid glands from 21 patients undergoing operations for primary hyperparathyroidism were imaged immediately after excision. CRM images were compared with conventional hematoxylin-and-eosin stained sections obtained from the same gland. The percentage area occupied by fat cells was calculated in images of both normal and diseased glands. RESULTS Characteristic microscopic features of parathyroid glands were distinguishable by CRM and correlated well with histopathology. The stromal fat content of normal and diseased glands could easily be determined. The percentage area occupied by fat cells differed significantly (P <.00001) in normal glands (average, 23.0% +/- 10.9%) and adenomatous glands (average, 0.4% +/- 0.7%). CONCLUSIONS CRM imaging rapidly revealed microscopic features that reliably differentiated normal and diseased parathyroid glands. The success of this preliminary ex vivo study promotes interest in further development of an in situ probe for in vivo clinical diagnostic use.

[1]  S. Geyer,et al.  The normal parathyroid gland at autopsy: The significance of stromal fat in adult patients , 1979, The Journal of pathology.

[2]  J. Norton,et al.  Prospective analysis of intraoperative and postoperative urinary cyclic adenosine 3',5'-monophosphate levels to predict outcome of patients undergoing reoperations for primary hyperparathyroidism. , 1988, Surgery.

[3]  A. Boyde,et al.  In vivo imaging of human teeth and skin using real-time confocal microscopy , 1991 .

[4]  Sheila J. Jones,et al.  Vital confocal microscopy in bone. , 2006, Scanning.

[5]  C. Wang Surgical management of primary hyperparathyroidism. , 1985, Current problems in surgery.

[6]  C. Proye,et al.  Multiglandular disease in seemingly sporadic primary hyperparathyroidism revisited: where are we in the early 1990s? A plea against unilateral parathyroid exploration. , 1992, Surgery.

[7]  R A Schuchard,et al.  Landmark-driven fundus perimetry using the scanning laser ophthalmoscope. , 1995, Investigative ophthalmology & visual science.

[8]  M. Rajadhyaksha,et al.  Confocal imaging of sebaceous gland hyperplasia in vivo to assess efficacy and mechanism of pulsed dye laser treatment , 1999, Lasers in surgery and medicine.

[9]  S. I. Roth,et al.  The rapid identification of "normal" parathyroid glands by the presence of intracellular fat. , 1976, The American journal of pathology.

[10]  R. Webb,et al.  Confocal scanning laser ophthalmoscope. , 1987, Applied optics.

[11]  E. Kaplan,et al.  Relation of postoperative hypocalcemia to operative techniques: deleterious effect of excessive use of parathyroid biopsy. , 1982, Surgery.

[12]  R. Webb,et al.  Spectrally encoded confocal microscopy. , 1998, Optics letters.

[13]  A. Dunn,et al.  Near real time confocal microscopy of cultured amelanotic cells: sources of signal, contrast agents and limits of contrast. , 1998, Journal of biomedical optics.

[14]  M Rajadhyaksha,et al.  Near-infrared confocal laser scanning microscopy of bladder tissue in vivo. , 1999, Urology.

[15]  R. Webb Confocal optical microscopy , 1996 .

[16]  R. Webb,et al.  In vivo confocal scanning laser microscopy of human skin II: advances in instrumentation and comparison with histology. , 1999, The Journal of investigative dermatology.

[17]  C. Murphy,et al.  The 20% rule: a simple, instantaneous radioactivity measurement defines cure and allows elimination of frozen sections and hormone assays during parathyroidectomy. , 1999, Surgery.

[18]  H. Ellis,et al.  Abdominal incisions and their closure. , 1985, Current problems in surgery.

[19]  S. Nussbaum,et al.  Intraoperative measurement of parathyroid hormone in the surgical management of hyperparathyroidism. , 1988, Surgery.

[20]  M Rajadhyaksha,et al.  Noninvasive Imaging of Human Oral Mucosa in Vivo by Confocal Reflectance Microscopy , 1999, The Laryngoscope.

[21]  H. D. Cavanagh,et al.  Tandem scanning confocal microscopy (TSCM) of normal and ischemic living kidneys. , 1991, The American journal of anatomy.

[22]  C. Wang,et al.  A Density Test for the Intraoperative Differentiation of Parathyroid Hyperplasia from Neoplasia , 1978, Annals of surgery.

[23]  D. Dufour,et al.  The normal parathyroid revisited: percentage of stromal fat. , 1982, Human pathology.

[24]  W M Petroll,et al.  Clinical and diagnostic use of in vivo confocal microscopy in patients with corneal disease. , 1993, Ophthalmology.

[25]  R. Webb,et al.  In vivo confocal scanning laser microscopy of human skin: melanin provides strong contrast. , 1995, The Journal of investigative dermatology.