CC BY 4.0 · Journal of Digestive Endoscopy 2023; 14(01): 051-055
DOI: 10.1055/s-0042-1759510
Case Report

Endoscopic Submucosal Dissection for Esophageal Squamous Cell High-grade Dysplasia in a Patient with Plummer Vinson Syndrome

1   Baldota Institute of Digestive Sciences, Gleneagles Global Hospital, Mumbai, Maharashtra, India
,
Amol Vadgaonkar
1   Baldota Institute of Digestive Sciences, Gleneagles Global Hospital, Mumbai, Maharashtra, India
,
1   Baldota Institute of Digestive Sciences, Gleneagles Global Hospital, Mumbai, Maharashtra, India
,
Sanil Parekh
1   Baldota Institute of Digestive Sciences, Gleneagles Global Hospital, Mumbai, Maharashtra, India
,
Animesh Shah
1   Baldota Institute of Digestive Sciences, Gleneagles Global Hospital, Mumbai, Maharashtra, India
,
Poorva Haridas
1   Baldota Institute of Digestive Sciences, Gleneagles Global Hospital, Mumbai, Maharashtra, India
,
Prajakta Gupte
2   Department of Pathology, HBT Medical College and Dr. R N Cooper Hospital, Mumbai, Maharashtra, India
,
Sehajad Vora
1   Baldota Institute of Digestive Sciences, Gleneagles Global Hospital, Mumbai, Maharashtra, India
,
1   Baldota Institute of Digestive Sciences, Gleneagles Global Hospital, Mumbai, Maharashtra, India
› Author Affiliations
Funding None.
 

Abstract

A 35-year female with Plummer Vinson syndrome (PVS) presented with a history of progressive dysphagia over six months, not responding to iron therapy and endoscopic dilatations. Her upper gastrointestinal endoscopy showed a post-cricoid web dilated using a Savary-Gilliard dilator. On NBI, a long segment circumferential lesion with abnormal microvascular architecture was noted in the mid esophagus. Biopsy showed high-grade dysplastic squamous epithelium. The patient underwent minimally invasive, circumferential endoscopic submucosal dissection (ESD) and received oral prednisolone to prevent stricture formation. Resected margins were free of dysplasia. At follow-up there was no evidence of recurrence or stricture formation. To our knowledge, this is the first case of PVS with squamous proliferation with high-grade dysplasia that was successfully treated with circumferential ESD. Screening endoscopy helps in the downstaging of early cancer, and timely intervention helps to treat this with a minimally invasive approach like ESD.


#

Introduction

Dysphagia to the passage of solids and liquids is an alarming symptom that needs timely evaluation and appropriate therapy.[1] Characterizing the symptoms will help differentiate esophageal dysphagia from oropharyngeal dysphagia.[2] Plummer-Vinson Syndrome (PVS) is identified by the presence of iron deficiency anemia (IDA), post-cricoid dysphagia, and esophageal web.[3] [4] It is commonly seen among middle-aged women and rarely in children and adolescents.[5] [6] Patients with esophageal rings or webs are usually asymptomatic. Symptomatic patients typically present with intermittent dysphagia to solids. The esophageal webs can rupture easily when the endoscope traverses the web. Dysphagia to solids due to strictures in the esophagus may need dilatation.[7] The prevalence of PVS seems to have lowered due to early detection and treatment of underlying IDA. PVS recognition is vital to identify patients with an increased risk of squamous cell carcinoma of the pharynx and esophagus; hence is considered a precancerous disease.[8] The frequency of post-cricoid carcinoma varies from 4–16% across studies.[4] [9] [10] If diagnosed early, patients with esophageal cancer can be treated with esophagectomy or minimally invasive endoscopic resection.[11] [12] Herein, we present a unique case of PVS with superficial squamous proliferation with high-grade dysplasia in the mid esophagus, which was treated successfully with endoscopic submucosal dissection (ESD).


#

The Case

A 35-year female presented with progressive dysphagia to solids dysphagia to solids (Grade 2) associated with weight loss of ∼10 kg in the last 6 months. An upper gastrointestinal endoscopy had initially shown post cricoid web ([Fig. 1]), dilated with CRE Wireguided Balloon Dilation (Boston Scientific, USA) done up to 12mm. The patient received oral iron supplements, pantoprazole 40mg, and sucralfate. However, her dysphagia was progressive; hence she showed up for an endoscopic procedure. The hemoglobin was 9.2 g/dl, the mean corpuscular volume was 60.6 fL, the white blood cell count was 9500/μl, and the platelet count was 450 × 103/μl. At presentation, patient had IDA (serum iron 10 μg/dL, total iron-binding capacity 450 μg/dL, transferrin saturation 5.5%). Endoscopy showed post-cricoid web, which was negotiated using a Savary-Gilliard (Cook Medical, USA) dilator. At 25cms from the incisors, a flat circumferential lesion was seen extending up to 35cms. The lesion was flat (Paris O-IIa) and showed altered surface contour on the mucosal aspect without any elevated or ulcerated areas on white light imaging. On Narrow band imaging and magnification, areas of dilated interpapillary capillary loops (IPCL-B1 pattern – Magnified endoscopic classification of JES) with loop formation were noted. Lugols iodine was sprayed, and biopsy was taken from unstained areas, suggesting squamous proliferation with high-grade dysplasia. A computed tomography scan showed no evidence of thickening of the esophagus, local nodes, or metastatic disease. After discussing the available treatment modalities, the patient was planned for a circumferential ESD.

Zoom Image
Fig. 1 (A) Post-cricoid web. (B) Post-cricoid web dilated with CRE Wireguided Balloon Dilation. (C) A flat circumferential lesion seen in esophagus extending up to 35cms. (D-F) Narrow band imaging showing areas of dilated interpapillary capillary loops (IPCL-B1 pattern – Magnified endoscopic classification of JES).

Under general anesthesia, with the patient in a supine position, the proximal and distal end of the lesion were marked using a Dual knife (Olympus, Tokyo, Japan) with a force-coagulation mode (effect 2, 40W) (VIO300D, ERBE Germany). A distal circumferential mucosal incision was done using a Dual knife (Olympus, Tokyo, Japan) (Endo Cut I) (Effect 2, Duration 3, Interval 3) after creating a submucosal cushion with saline and methylene blue with an endoscopic injection needle (NM-400L, Olympus, USA). The submucosal fibers were dissected to expose the muscularis all along the distal part of the lesion ([Fig. 2]). After that, a mucosal incision was done along the proximal aspect of the lesion on the posterior esophageal wall. The submucosal dissection was performed with a force-coagulation mode (effect 2, 40W), and a submucosal tunnel was created to join the proximal and distal mucosal incision. Another similar submucosal tunnel was created along the anterior aspect of the lesion. Both the tunnels were joined by lateral dissection, and the entire dysplastic area was meticulously resected en block (∼6 cm) and submitted for a histopathology examination. Hemostasis was achieved with Coagrasper Hemostatic forceps (FD-410LR, Olympus, USA) using forced coagulation (60W). The procedure time was 210 mins. Postoperatively the patient was kept nil by mouth, and iv fluids were given. She had a low-grade fever which settled with paracetamol and antibiotics (cefixime). On the third postoperative day patient was started on clear liquids, which were tolerated well, and oral steroids (prednisolone 30mg daily) on tapering dosage for prevention of esophageal stricture. On Day 5 patient was discharged on liquids.

Zoom Image
Fig. 2 (A-D) Circumferential mucosal incision was done and submucosal fibers dissected. Submucosal tunnel was created to join the proximal and distal mucosal incision. Another submucosal tunnel was created along the anterior aspect, both tunnels joined by lateral dissection, and the entire dysplastic lesion was resected en block. (E) Narrowing at 35cm from the incisors (1 month). (F) Follow up endoscopy at 6 months. (G) High-grade squamous dysplasia confined to the muscularis mucosa (inset showing specimen of resected lesion ∼6cms). (H) Vertical margins negative, no lymphovascular invasion.

Biopsy was suggestive of high-grade squamous dysplasia confined to the muscularis mucosa (T1a), the vertical margins were negative, and there was no lymphovascular invasion. At follow-up endoscopy (1 month), the previous ESD site showed scarring with neovascularization. Healthy granulation tissue surrounding the ESD site was seen. There was a narrowing at 35cm from the incisors. CRE Wireguided Balloon Dilation (Boston Scientific, USA) was done up to 11mm; the scope was then negotiated across the stricture. The patient was encouraged to eat a well-balanced and nutritious diet. On follow-up at 6 months, the patient has gained weight, is tolerating an oral diet, and has no history of dysphagia or recurrence of the disease.


#

Discussion

The pathogenesis of PVS remains largely unknown. The most plausible etiologic factor is IDA which can precede dysphagia. The gastrointestinal tract is susceptible to iron deficiency leading to mucosa degeneration and web formation.[13] These factors were also noted in our patient. Other etiologic factors such as genetic predisposition and malnutrition, are considered.[14] These can be missed due to their proximity to the upper esophageal sphincter. PVS is managed with iron supplementation, but severe obstruction by the esophageal web needs mechanical dilation. A single dilation helps treat dysphagia in most cases, but recurrent dysphagia is seen in those with an esophageal ring. In a study of 33 patients after dilation of an esophageal ring, recurrent dysphagia was reported in 89% of patients at 5 years.[15] The patients must be followed closely as there is a high chance of recurrence. Surveillance endoscopy can be performed yearly, though no definitive recommendation exists.

The occurrence of esophageal cancer is increasing, and as per GLOBOCAN 2020 estimates, it ranks seventh and sixth in terms of incidence and overall mortality, respectively.[16] ESD is an excellent modality for patients with early cancer but not advanced tumors. It utilizes endoscopic tools to dissect lesions from the submucosa like superficial esophageal cancer or those with high-grade dysplasia.[17] [18] So, ESD was chosen as the mode of therapy for this patient. Several studies have shown low mortality rates following ESD of isolated lesions. ESD helps to perform en bloc resection for histopathologic assessment. Five-year survival rates range from 76 to 100%.[19] [20] However, survival is lower in patients with lesions that extend beyond the lamina propria. Recurrences have been seen in 3 to 32% of patients.

Adverse events of ESD include mediastinal emphysema (suggesting perforation), ulcer bleeding, and esophageal stricture.[21] Strictures are typically seen in patients with a mucosal defect involving more than three-fourths of the esophageal circumference. Triamcinolone injection during resection may decrease the risk of stricture formation. Strictures are typically treated with esophageal balloon dilation.[22] We embarked on using a tunnel creation technique based on submucosal dissection principles performed during POEM. This technique was quicker than conventional ESD, and the lesion could be dissected easily without muscle injury. Steroid administration with either topical or local injection prevents stricture formation. In a small retrospective series, treating with esophageal balloon dilation plus an oral steroid was associated with a reduced need for esophageal balloon dilation compared with the sole exception. ESD and esophagectomy were studied in patients with early esophageal squamous cell carcinoma. ESD outcome was comparable to esophagectomy with minimal invasion, lower cost, and serious adverse events. ESD could act as a first-line modality for T1a-M1/M2 and T1b-M3/SM1 esophageal carcinoma. However, esophagectomy may be preferable in those with SM2/SM3.[23] Surgery and chemoradiotherapy should be recommended for lymphovascular involvement or submucosal invasion. A head-to-head outcome comparison with esophagectomy in patients with PVS is currently unavailable.

A retrospective study over 18 years studied 135 patients with PVS; 86% were women with a mean age of 42 years; the common symptom was dysphagia. Mid and distal esophageal cancers were more common. The mean interval between diagnosis of PVS and squamous cell carcinoma was 6 years.[24] Patil M et al. studied 132 cases of PVS over a 10-year period in which 4 patients showed concomitant esophageal tumors post dilatation of post cricoid web. Upper esophageal malignancy was seen in 4.5% of patients. ESD is now gaining popularity in Scandinavian countries for gastric lesions.[25] Misjudgment of the indications or curability assessment can result in unfavorable patient outcomes.

To summarize, the present case of PVS was treated successfully with circumferential ESD. The procedure was safe to perform and effective in treating high-grade dysplasia. ESD may provide a non-surgical treatment option for patients with advanced tumors, which needs to be explored in well-designed controlled trials.


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Conflict of Interest

None declared.

Acknowledgments

We thank Dr. Rajen Daftary for his dedicated anesthesia care during the procedure. We thank Mr. Milind Jadhav for editing the pictures to suit journal requirements.

Presentation at a Meeting

Not presented.


Author Contributions

Concept – GP; Design –GP, AV; Performed case – GP, SV; Data Collection and/or Processing –GP, AV; Literature Review- AD, PH, AS, SP; Performed histopathological analysis – PG; Writing – AS, AV, GP; Critical Reviews - AM.


All the authors reviewed and approved the final version of the manuscript.


Consent

Consent from the patient was obtained regarding the publication of this case.


  • References

  • 1 Philpott H, Garg M, Tomic D, Balasubramanian S, Sweis R. Dysphagia: Thinking outside the box. World J Gastroenterol 2017; 23 (38) 6942-6951
  • 2 Rommel N, Hamdy S. Oropharyngeal dysphagia: manifestations and diagnosis. Nat Rev Gastroenterol Hepatol 2016; 13 (01) 49-59
  • 3 Goel A, Lakshmi CP, Bakshi SS, Soni N, Koshy S. Single-center prospective study of Plummer-Vinson syndrome. Dis Esophagus 2016; 29 (07) 837-841
  • 4 Patil M, Malipatel R, Devarbhavi H. Plummer-Vinson syndrome: A decade's experience of 132 cases from a single center. J Gastroenterol Hepatol 2021; 36 (01) 181-185
  • 5 Harmouch F, Liaquat H, Chaput KJ, Geme B. Plummer-Vinson Syndrome: A Rare Cause of Dysphagia in an Octogenarian. Am J Case Rep 2021; 22: e929899
  • 6 Mansell NJ, Jani P, Bailey CM. Plummer-Vinson syndrome–a rare presentation in a child. J Laryngol Otol 1999; 113 (05) 475-476
  • 7 Sreenivas DV, Kumar A, Mannar KV, Babu GR. Results of Savary-Gilliard dilatation in the management of cervical web of esophagus. Hepatogastroenterology 2002; 49 (43) 188-190
  • 8 Goel A, Bakshi SS, Soni N, Chhavi N. Iron deficiency anemia and Plummer-Vinson syndrome: current insights. J Blood Med 2017; 8 (08) 175-184
  • 9 Larsson LG, Sandström A, Westling P. Relationship of Plummer-Vinson disease to cancer of the upper alimentary tract in Sweden. Cancer Res 1975; 35 (11 Pt. 2): 3308-3316
  • 10 Mohan P, Munisamy M, Selvan KS, Hamide A. Esophageal squamous cell cancer in Plummer-Vinson syndrome: Is lichen planus a missing link?. J Postgrad Med 2022; 68 (02) 98-99
  • 11 Sewnaik A, Hoorweg JJ, Knegt PP, Wieringa MH, van der Beek JM, Kerrebijn JD. Treatment of hypopharyngeal carcinoma: analysis of nationwide study in the Netherlands over a 10-year period. Clin Otolaryngol 2005; 30 (01) 52-57
  • 12 Probst A, Aust D, Märkl B, Anthuber M, Messmann H. Early esophageal cancer in Europe: endoscopic treatment by endoscopic submucosal dissection. Endoscopy 2015; 47 (02) 113-121
  • 13 Geerlings SE, Statius van Eps LW. Pathogenesis and consequences of Plummer-Vinson syndrome. Clin Investig 1992; 70 (08) 629-630
  • 14 Nasa M, Patil G, Sharma Z, Puri R. Plummer-Vinson Syndrome with Simultaneous Mid-esophageal Growth. J Assoc Physicians India 2017; 65 (02) 96-97
  • 15 Eckardt VF, Kanzler G, Willems D. Single dilation of symptomatic Schatzki rings. A prospective evaluation of its effectiveness. Dig Dis Sci 1992; 37 (04) 577-582
  • 16 Sung H, Ferlay J, Siegel RL. et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin 2021; 71 (03) 209-249
  • 17 Wang KK, Prasad G, Tian J. Endoscopic mucosal resection and endoscopic submucosal dissection in esophageal and gastric cancers. Curr Opin Gastroenterol 2010; 26 (05) 453-458
  • 18 Aabakken L. Endoscopic diagnosis and treatment of tumors. Endoscopy 2009; 41 (10) 861-865
  • 19 Ning B, Abdelfatah MM, Othman MO. Endoscopic submucosal dissection and endoscopic mucosal resection for early stage esophageal cancer. Ann Cardiothorac Surg 2017; 6 (02) 88-98
  • 20 Aadam AA, Abe S. Endoscopic submucosal dissection for superficial esophageal cancer. Dis Esophagus 2018; 31(07):
  • 21 Joo DC, Kim GH, Park DY, Jhi JH, Song GA. Long-term outcome after endoscopic submucosal dissection in patients with superficial esophageal squamous cell carcinoma: a single-center study. Gut Liver 2014; 8 (06) 612-618
  • 22 Qi L, He W, Yang J, Gao Y, Chen J. Endoscopic balloon dilation and submucosal injection of triamcinolone acetonide in the treatment of esophageal stricture: A single-center retrospective study. Exp Ther Med 2018; 16 (06) 5248-5252
  • 23 An W, Liu MY, Zhang J. et al. Endoscopic submucosal dissection versus esophagectomy for early esophageal squamous cell carcinoma with tumor invasion to different depths. Am J Cancer Res 2020; 10 (09) 2977-2992
  • 24 Bakari G, Benelbarhdadi I, Bahije L, El Feydi Essaid A. Endoscopic treatment of 135 cases of Plummer-Vinson web: a pilot experience. Gastrointest Endosc 2014; 80 (04) 738-741
  • 25 Rushfeldt C, Aabakken L. Implementation of Endoscopic Submucosal Dissection for Gastric Lesions in Norway. Scand J Surg 2016; 105 (02) 90-96

Address for correspondence

Gaurav Patil, MBBS, DNB(Med), DNB (Gastro)
Baldota Institute of Digestive Sciences, Gleneagles Global Hospitals
Mumbai, Maharashtra
India – 400012

Publication History

Article published online:
23 December 2022

© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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  • References

  • 1 Philpott H, Garg M, Tomic D, Balasubramanian S, Sweis R. Dysphagia: Thinking outside the box. World J Gastroenterol 2017; 23 (38) 6942-6951
  • 2 Rommel N, Hamdy S. Oropharyngeal dysphagia: manifestations and diagnosis. Nat Rev Gastroenterol Hepatol 2016; 13 (01) 49-59
  • 3 Goel A, Lakshmi CP, Bakshi SS, Soni N, Koshy S. Single-center prospective study of Plummer-Vinson syndrome. Dis Esophagus 2016; 29 (07) 837-841
  • 4 Patil M, Malipatel R, Devarbhavi H. Plummer-Vinson syndrome: A decade's experience of 132 cases from a single center. J Gastroenterol Hepatol 2021; 36 (01) 181-185
  • 5 Harmouch F, Liaquat H, Chaput KJ, Geme B. Plummer-Vinson Syndrome: A Rare Cause of Dysphagia in an Octogenarian. Am J Case Rep 2021; 22: e929899
  • 6 Mansell NJ, Jani P, Bailey CM. Plummer-Vinson syndrome–a rare presentation in a child. J Laryngol Otol 1999; 113 (05) 475-476
  • 7 Sreenivas DV, Kumar A, Mannar KV, Babu GR. Results of Savary-Gilliard dilatation in the management of cervical web of esophagus. Hepatogastroenterology 2002; 49 (43) 188-190
  • 8 Goel A, Bakshi SS, Soni N, Chhavi N. Iron deficiency anemia and Plummer-Vinson syndrome: current insights. J Blood Med 2017; 8 (08) 175-184
  • 9 Larsson LG, Sandström A, Westling P. Relationship of Plummer-Vinson disease to cancer of the upper alimentary tract in Sweden. Cancer Res 1975; 35 (11 Pt. 2): 3308-3316
  • 10 Mohan P, Munisamy M, Selvan KS, Hamide A. Esophageal squamous cell cancer in Plummer-Vinson syndrome: Is lichen planus a missing link?. J Postgrad Med 2022; 68 (02) 98-99
  • 11 Sewnaik A, Hoorweg JJ, Knegt PP, Wieringa MH, van der Beek JM, Kerrebijn JD. Treatment of hypopharyngeal carcinoma: analysis of nationwide study in the Netherlands over a 10-year period. Clin Otolaryngol 2005; 30 (01) 52-57
  • 12 Probst A, Aust D, Märkl B, Anthuber M, Messmann H. Early esophageal cancer in Europe: endoscopic treatment by endoscopic submucosal dissection. Endoscopy 2015; 47 (02) 113-121
  • 13 Geerlings SE, Statius van Eps LW. Pathogenesis and consequences of Plummer-Vinson syndrome. Clin Investig 1992; 70 (08) 629-630
  • 14 Nasa M, Patil G, Sharma Z, Puri R. Plummer-Vinson Syndrome with Simultaneous Mid-esophageal Growth. J Assoc Physicians India 2017; 65 (02) 96-97
  • 15 Eckardt VF, Kanzler G, Willems D. Single dilation of symptomatic Schatzki rings. A prospective evaluation of its effectiveness. Dig Dis Sci 1992; 37 (04) 577-582
  • 16 Sung H, Ferlay J, Siegel RL. et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin 2021; 71 (03) 209-249
  • 17 Wang KK, Prasad G, Tian J. Endoscopic mucosal resection and endoscopic submucosal dissection in esophageal and gastric cancers. Curr Opin Gastroenterol 2010; 26 (05) 453-458
  • 18 Aabakken L. Endoscopic diagnosis and treatment of tumors. Endoscopy 2009; 41 (10) 861-865
  • 19 Ning B, Abdelfatah MM, Othman MO. Endoscopic submucosal dissection and endoscopic mucosal resection for early stage esophageal cancer. Ann Cardiothorac Surg 2017; 6 (02) 88-98
  • 20 Aadam AA, Abe S. Endoscopic submucosal dissection for superficial esophageal cancer. Dis Esophagus 2018; 31(07):
  • 21 Joo DC, Kim GH, Park DY, Jhi JH, Song GA. Long-term outcome after endoscopic submucosal dissection in patients with superficial esophageal squamous cell carcinoma: a single-center study. Gut Liver 2014; 8 (06) 612-618
  • 22 Qi L, He W, Yang J, Gao Y, Chen J. Endoscopic balloon dilation and submucosal injection of triamcinolone acetonide in the treatment of esophageal stricture: A single-center retrospective study. Exp Ther Med 2018; 16 (06) 5248-5252
  • 23 An W, Liu MY, Zhang J. et al. Endoscopic submucosal dissection versus esophagectomy for early esophageal squamous cell carcinoma with tumor invasion to different depths. Am J Cancer Res 2020; 10 (09) 2977-2992
  • 24 Bakari G, Benelbarhdadi I, Bahije L, El Feydi Essaid A. Endoscopic treatment of 135 cases of Plummer-Vinson web: a pilot experience. Gastrointest Endosc 2014; 80 (04) 738-741
  • 25 Rushfeldt C, Aabakken L. Implementation of Endoscopic Submucosal Dissection for Gastric Lesions in Norway. Scand J Surg 2016; 105 (02) 90-96

Zoom Image
Fig. 1 (A) Post-cricoid web. (B) Post-cricoid web dilated with CRE Wireguided Balloon Dilation. (C) A flat circumferential lesion seen in esophagus extending up to 35cms. (D-F) Narrow band imaging showing areas of dilated interpapillary capillary loops (IPCL-B1 pattern – Magnified endoscopic classification of JES).
Zoom Image
Fig. 2 (A-D) Circumferential mucosal incision was done and submucosal fibers dissected. Submucosal tunnel was created to join the proximal and distal mucosal incision. Another submucosal tunnel was created along the anterior aspect, both tunnels joined by lateral dissection, and the entire dysplastic lesion was resected en block. (E) Narrowing at 35cm from the incisors (1 month). (F) Follow up endoscopy at 6 months. (G) High-grade squamous dysplasia confined to the muscularis mucosa (inset showing specimen of resected lesion ∼6cms). (H) Vertical margins negative, no lymphovascular invasion.