Foregut duplication cyst presenting as lingual swelling: Case report and review of literature

Hambarde, Sandeep; Bendre, Pradnya; Taide, Devendra

doi:10.4103/0975-5950.85844

Cited by 14 publications

(7 citation statements)

References 12 publications

(31 reference statements)

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“…In previous reports of lingual heterotopic gastrointestinal cysts, intubation was required for airway management in three of nine cases[ 6 , 7 ]. The remaining seven patients were not intubated, as ultrasonographic imaging showed that there were no airway problems[ 4 , 5 , 8 - 10 ]. Preoperative aspiration or marsupialization was performed in four cases, while aspiration alone was performed in two cases[ 5 , 6 , 9 ].…”

Section: Discussionmentioning

confidence: 99%

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Large lingual heterotopic gastrointestinal cyst in a newborn: A case report

Lee

Harada

Tanaka

et al. 2020

WJCC

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BACKGROUND Heterotopic gastrointestinal cysts have gastrointestinal epithelium in the cyst wall and rarely occur in the oral cavity. Most are found in the neonatal period. However, heterotopic gastrointestinal cysts that are diagnosed as a congenital tongue cyst by routine ultrasonography are extremely rare. CASE SUMMARY A 12-day-old female presented with swelling of the anterior tongue. The obstetrician had detected significant tongue swelling on fetal ultrasonography in the 35 th gestational week. The female was born by cesarean delivery at gestational week 39. She soon became dyspneic, and the cyst was aspirated. After the aspiration, her breathing recovered and she started breastfeeding. The cyst was excised under general anesthesia on the 67 th day. Histopathologic examination showed that that cyst wall consisted of a lining of columnar gastrointestinal-type epithelium and pseudostratified ciliated epithelium. The patient restarted breastfeeding 3 h after surgery. The postoperative course was uneventful. CONCLUSION Airway distress and feeding difficulty were successfully avoided by cyst aspiration, and surgical resection was performed with no perioperative complications.

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Section: Discussionmentioning

confidence: 99%

“…Congenital tongue cysts can cause respiratory distress and require multidisciplinary treatment for airway management. Intratracheal intubation and reduction procedures may be required immediately after delivery[ 5 - 7 , 9 ]. The treatment is complete surgical resection, and there are very few cases of recurrence[ 2 ].…”

Section: Introductionmentioning

confidence: 99%

Large lingual heterotopic gastrointestinal cyst in a newborn: A case report

Lee

Harada

Tanaka

et al. 2020

WJCC

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“…Larger cysts present with dyspnea or dysphagia and symptoms are generally more acute. Although fine-needle aspiration of the cyst content can give temporary relief during the neonatal period, definitive treatment can only be achieved by total excision of the cyst via laser ablation or bipolar diathermy [1, 10, 11]. …”

Section: Discussionmentioning

confidence: 99%

Enteric Duplication Cyst Located at the Posterior Tongue: A Rare Case Report and Review of the Literature

Savran

Kucur

Koçak

et al. 2015

Case Reports in Otolaryngology

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The lingual localization of an enteric duplication is extremely rare but may present with respiratory and feeding problems that require emergency intervention. A 7-month-old boy was brought to our clinic with feeding difficulties and tongue swelling. Physical examination showed a cystic lesion located near the left side of the tongue base that caused tongue protrusion to the contralateral side. During surgery, a 3-cm diameter opaque thick-walled cyst was found to be very closely adherent to the base of tongue, which was excised in its entirety. Following surgery, the patient fed during the early postoperative period and no complications were observed other than hypersalivation. On histological examination, a cystic lesion lined with intestinal mucosa and goblet cells was found. We present the rare case of a duplication cyst of the posterior tongue, with a literature review.

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“…Enteric duplication cysts are congenital malformations that are found anywhere from the mouth to the anus 1 2 910.…”

Section: Discussionmentioning

confidence: 99%

A retroperitoneal enteric duplication cyst communicating with the right upper ureter in an infant

et al. 2014

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SUMMARYWe report an extremely rare case of isolated retroperitoneal enteric duplication cyst with gastric mucosa causing haematuria and dysuria by communicating with the urinary system. A 9-month-old male child was admitted to our hospital with persistent haematuria, dysuria and anaemia. Investigations revealed a retroperitoneal cyst abutting the hydronephrotic nonfunctioning right kidney. At surgery an isolated retroperitoneal cyst communicating with the right pelviureteric junction was found. The kidney and associated cyst were excised. Histology of the cystic lesion revealed an enteric duplication cyst lined by ectopic gastric mucosa. Isolated retroperitoneal enteric duplication cyst communicating with the urinary tract has not been previously reported in the English literature. We propose that acid secretion into the right renal system was the cause of the haematuria-dysuria syndrome which promptly resolved postoperatively. BACKGROUND

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Foregut duplication cyst presenting as lingual swelling: Case report and review of literature

Cited by 14 publications

References 12 publications

Large lingual heterotopic gastrointestinal cyst in a newborn: A case report

Large lingual heterotopic gastrointestinal cyst in a newborn: A case report

Enteric Duplication Cyst Located at the Posterior Tongue: A Rare Case Report and Review of the Literature

A retroperitoneal enteric duplication cyst communicating with the right upper ureter in an infant

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