Can someone help me with the following please?
1. Wide local excision of the right helix and lobule.
2. Closure of irregular defect with local advancement flaps.
3. Sentinel lymph node biopsy using lymphoscintigraphy and Lymphazurin
lymphatic dye.
wide local excision and sentinel lymph node biopsy. Review of the images
was undertaken prior to entering the OR. The patient localized well to two
sites in the right neck, one in level 2A and the other in 5B. These sites
were marked on the neck. The patient was brought to the operating facility
after correct identification. Operative time-out was performed. The
patient was then prepped and draped in the usual sterile fashion. Prior to
prepping and draping 1 mL of Lymphazurin dye was injected into the helix in
the region of the melanoma excision around the circumferential area.
Following prepping and draping a wide local excision in the form of wedge
resection of the helix and superior lobule was undertaken. This was closed
primarily by advancing the lobule and the helical segments with closure
with deep 3-0 Vicryl followed by a running 5-0 plain gut stitch. Following
this attention was turned to the two sites marked status post
lymphoscintigraphy. Baseline radioactivity was measured with the Geiger
counter. Of note, prior to excision of the primary background was 40 and
the primary site measure 4300. Prior to incising sentinel lymph node
biopsy site 1 the baseline was 1200. Blunt dissection was used since this
was in the region of the marginal mandibular nerve in level 2A to take
every precaution and using nerve safe dissection techniques. Burlisher as
well as Bovie cautery was used to dissect. Dissection was carried through
the incision site down to the level of the retromandibular vein. At this
point Lymphazurin dye was readily visible. Specimen was removed. Ex vivo
measurement with a Geiger counter revealed an activity of 9800 of the ex
vivo specimen. The excisional site dropped in activity from 1200 at
baseline to 500 status post removal of the specimen. There was a
superficial specimen that was removed and placed in a separate specimen cup
prior to the Lymphazurin and positive double collection. This extra
sentinel lymph node segment measured a total of 40. Following this
attention was turned to the second sentinel lymph node site. Baseline for
this site was 2200. Again dissection was carried down using Burlisher and
Bovie cautery. A Weitlaner was used for retraction as well as a Cummings
retractor for exposure. The specimen was removed which we felt was a good
cluster of benign-appearing lymph nodes. The ex vivo measurement was 1900.
Following this the sentinel node site was measured and the baseline of 2200
had dropped to 10 which we were satisfied with. Closure of the two
sentinel lymph node sites was performed with interrupted Vicryl and
running subcuticular Monocryl. The patient tolerated the procedure very
1. Wide local excision of the right helix and lobule.
2. Closure of irregular defect with local advancement flaps.
3. Sentinel lymph node biopsy using lymphoscintigraphy and Lymphazurin
lymphatic dye.
wide local excision and sentinel lymph node biopsy. Review of the images
was undertaken prior to entering the OR. The patient localized well to two
sites in the right neck, one in level 2A and the other in 5B. These sites
were marked on the neck. The patient was brought to the operating facility
after correct identification. Operative time-out was performed. The
patient was then prepped and draped in the usual sterile fashion. Prior to
prepping and draping 1 mL of Lymphazurin dye was injected into the helix in
the region of the melanoma excision around the circumferential area.
Following prepping and draping a wide local excision in the form of wedge
resection of the helix and superior lobule was undertaken. This was closed
primarily by advancing the lobule and the helical segments with closure
with deep 3-0 Vicryl followed by a running 5-0 plain gut stitch. Following
this attention was turned to the two sites marked status post
lymphoscintigraphy. Baseline radioactivity was measured with the Geiger
counter. Of note, prior to excision of the primary background was 40 and
the primary site measure 4300. Prior to incising sentinel lymph node
biopsy site 1 the baseline was 1200. Blunt dissection was used since this
was in the region of the marginal mandibular nerve in level 2A to take
every precaution and using nerve safe dissection techniques. Burlisher as
well as Bovie cautery was used to dissect. Dissection was carried through
the incision site down to the level of the retromandibular vein. At this
point Lymphazurin dye was readily visible. Specimen was removed. Ex vivo
measurement with a Geiger counter revealed an activity of 9800 of the ex
vivo specimen. The excisional site dropped in activity from 1200 at
baseline to 500 status post removal of the specimen. There was a
superficial specimen that was removed and placed in a separate specimen cup
prior to the Lymphazurin and positive double collection. This extra
sentinel lymph node segment measured a total of 40. Following this
attention was turned to the second sentinel lymph node site. Baseline for
this site was 2200. Again dissection was carried down using Burlisher and
Bovie cautery. A Weitlaner was used for retraction as well as a Cummings
retractor for exposure. The specimen was removed which we felt was a good
cluster of benign-appearing lymph nodes. The ex vivo measurement was 1900.
Following this the sentinel node site was measured and the baseline of 2200
had dropped to 10 which we were satisfied with. Closure of the two
sentinel lymph node sites was performed with interrupted Vicryl and
running subcuticular Monocryl. The patient tolerated the procedure very