• Title/Summary/Keyword: Adenoid Cystic Carcinoma

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Two Cases of Adenoid Cystic Carcinoma of Trachea (기관내 선양낭성암종 2예)

  • Yum, Ho-Kee;Ahan, Jin-Chul;Song, Yeong-Soo;Kim, Joo-In;Yoon, Hye-Kyoung;Jeon, Woo-Ki;Choi, Soo-Jeon;Lee, Bong-Choon
    • Tuberculosis and Respiratory Diseases
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    • v.42 no.3
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    • pp.387-393
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    • 1995
  • Adenoid cystic carcinoma formerly called cylindroma is rare tracheal tumor. Characteristics of adenoid cystic carcinoma are infiltrative nature with local recurrence tendency and long natural course of the disease. Adenoid cystic carcinomas develop most commonly in the trachea. Primary resection and end-to-end anastomosis of the involved airway are treatment of choice. And postoperative radiation therapy might be useful, particularly when the surgical margins are not ample. We report two cases of adenoid cystic carcinoma of trachea diagnosed by flow-volume curve.

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A Case of Primary Cutaneous Adenoid Cystic Carcinoma at the Genital Area (외음부에 발생한 원발성 피부 선상 낭종성 암의 치험례)

  • Jeong, Hoi Joon;Son, Dae Gu;Kwon, Sun Young
    • Archives of Plastic Surgery
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    • v.35 no.3
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    • pp.333-336
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    • 2008
  • Purpose: Adenoid cystic carcinoma is a rare type of eccrine sweat gland carcinoma. Although it is mostly known as a neoplasm of the salivary gland, it could occur as a primary skin tumor. We present a patient with a primary cutaneous adenoid cystic carcinoma at the genital area. Methods: A 60-year-old man had a slowly growing 1 cm sized single tender mass near the left scrotum and he underwent excisional biopsy at a local clinic. A diagnosis of adenoid cystic carcinoma was made and thus he was transferred to our hospital. In physical examination, other specific findings were not detected except a linear scar caused by a previous skin biopsy near the left scrotum. In CT scan, PET-CT scan and endoscopy, there was no evidence of neoplasm in other organs. It was diagnosed as the primary cutaneous adenoid cystic carcinoma and then wide excisions were performed including total 4.5 cm margin of normal skin. Results: Microscopic findings revealed proliferation of tumor cell islands with cribriform or tubular patterns containing several round, pseudocystic structures. The tumor cells showed basaloid cells with uniform and small nuclei. Tumor cells infiltrated into the dermis and upper portion of subcutaneous tissue. There was multifocal perineural invasion of tumor cells. In postoperative 6 months, we found no recurrence and other complications. Conclusion: Herein we found a rare case of primary cutaneous adenoid cystic carcinoma at the genital area.

Adenoid cystic carcinoma presenting as an ulcer on the floor of the mouth: a rare case report

  • Khan, Saba;Agwani, Khalid;Bhargava, Puneet;Kumar, Sreeja P.
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • v.40 no.5
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    • pp.253-257
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    • 2014
  • Adenoid cystic carcinoma is a rare epithelial tumour, and comprises about 1% of all malignant tumours of the oral and maxillofacial region. It is a malignant tumour which may develop in the trachea, bronchus, lungs or mammary glands, in addition to the head and neck region. Occurrences in the head and neck are mostly detected in the major salivary gland, oral cavity, pharynx and paranasal sinus where it presents as a slow growing firm nodular swelling. The aim of the article is to highlight the unique presentation of adenoid cystic carcinoma as a solitary ulcer on the floor of the mouth.

Adenoid Cystic Carcinoma of the Esophagus - A case report - (식도 선낭포종양치험 1예)

  • 임승균
    • Journal of Chest Surgery
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    • v.20 no.4
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    • pp.865-868
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    • 1987
  • Adenoid cystic carcinoma of the esophagus has been relatively an uncommon, slow growing tumor. A 51 year-old man patient had a tumor in the lower third of the esophagus which was incidentally found during an examination for UPPER C-I series, and resected successfully without Thoracotomy. The tumor exhibited a polypoid appearance covered by normal esophageal epithelium, localized entirely in the submucosal layer of the esophagus and morphologically identical to adenoid cystic carcinoma in the salivary glands.

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A CASE REPORT OF CALCIFYING APONEUROTIC FIBROMA ACCOMPANIED BY ADENOID CYSTIC CARCINOMA (선상 낭포성 암종을 동반한 석회성 건막 섬유종의 치험예)

  • Kim, Il-Kyu;Oh, Seong-Seob
    • Maxillofacial Plastic and Reconstructive Surgery
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    • v.17 no.2
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    • pp.195-201
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    • 1995
  • This is a case report of calcifying aponeurotic fibroma occurred in the right pterygopalatine fossa & ramus area accompanied by adenoid cystic carcinoma of the right sublingual gland of a 44-year-old female. Calcifying aponeurotic fibroma is benign tumor, but it is characterized by poorly marginated, infiltrated growth pattern and a stubborn tendency to local recurrence, but there is no record of malignant transformation or metastasis, and surgical management should be conservative(excision and reexcision). Most cases been reported at the hands and feet, but no reported case occuring in the head region is found in the literature. Adenoid cystic carcinoma is a slow-growing infiltrative tumor with high recurrence rate, and it's treatment requires radical excisin and radiotherapy. Wide surgical excision of tumor, RND and partial resection of mandible were done. And then, immediate mandibular reconstruction was performed by means of reimplantaion technique after autoclaving of the resected bone.

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A Case of Adenoid Cystic Carcinoma of Sublingual Gland Forming a Major Sublingual Duct, which Empties into Wharton's Duct (악하선관으로 연결되는 주설하관을 가진 설하선과 이에 발생한 선양낭성암종 1례)

  • Moon, Sung-Joong;Jung, Young-Ho;Chang, Mee-Soo;Jin, Hong-Ryul
    • Korean Journal of Head & Neck Oncology
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    • v.22 no.2
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    • pp.171-174
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    • 2006
  • Tumors rarely arise in the sublingual salivary glands. They should be considered malignant until proved otherwise. Adenoid cystic carcinoma is most commonly encountered malignant tumor of the sublingual gland. We report a case of adenoid cystic carcinoma arising from the sublingual gland. Moreover, the sublingual gland had anatomic variation of main duct(Bartholin's duct) which is connected to Wharton's duct.

A case report A Case Report of Adenoid Cystic Carcinoma in Trachea (기관에 생긴 기관지선종 치험 1례)

  • Yoon, Yeo-Jun;Cho, Beom-Gu;Hong, Seung-Rok
    • Journal of Chest Surgery
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    • v.11 no.3
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    • pp.265-268
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    • 1978
  • Adenoid cystic carcinoma is rare and one of the bronchial adenoma. This is a case report of adenoid cystic carcinoma in a 28 years old female patient, which was treated surgically in chest surgery department of Severance hospital, Yonsei University. The tumor was located in cervical trachea with wide base and obstructing the lumen almost completely. The tumor was resected and End-to-End anastomosed. The tumor was confirmed to be adenoid cystic carcinoma histopathologically.

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Histopathologic Classification of Salivary Gland Neoplasm (경부기관에 발생한 선양낭성암종 1예)

  • 추호석;정은재;권순영;정광윤
    • Korean Journal of Bronchoesophagology
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    • v.9 no.1
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    • pp.75-78
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    • 2003
  • Primary adenoid cystic carcioma of trachea is rare, with an incidence of only 0.2 per 100,000 persons per year. When all series of the tracheal carcinomas are combined, adenoid cystic carcinoma is the second most common tumor only to squamous cell carcinoma in incidence. Most patients have wheezing or stridor, dyspnea, hemoptysis, and cough as symptoms. Treatment options include surgery alone, radiation therapy alone, or a combination of both. The recommended surgical option is primary tracheal resection and reconstruction. Recently, we experienced a case of adenoid cystic carcinoma in 45 year old female patient who was treated tracheal tumor resection and end-to-end anastomosis of the trachea, so we report this case with the literatures.

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A CASE REPORT OF ADENOID CYSTIC CARCINOMA OF THE MINOR SALIVARY GLAND IN RETROMOLAR PAD (좌측 하악 후삼각부에 발생한 선양 낭종암의 치험례)

  • Oh, Sang-Hwa;Kim, Woo-Hyung;Son, Yong-Jun;Kho, Young-Gui;Lee, Hee-Chul
    • Maxillofacial Plastic and Reconstructive Surgery
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    • v.17 no.4
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    • pp.389-395
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    • 1995
  • Adenoid cystic carcinoma is malignant neoplasm belonging to a group of tumors of salivary gland origin. It is an aggressive tumor characterized by slow growth and incidious destruction of surrounding tissues. Perineural invasion is a prominent feature. Spread to regional lymph node is rare, other than by direct extension. Distant metastasis are more common. We experienced a 65-year old female with adenoid cystic carcinoma of minor salivary gland in retromolar pad.

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Basal cell adenoma misdiagnosed as an adenoid cystic carcinoma in the parotid gland

  • Kim, Chan-Woo;Kim, Seong-Gon
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • v.38 no.5
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    • pp.314-317
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    • 2012
  • Basal cell adenoma (BCA) of the parotid gland is a rare benign tumor. In the parotid gland, BCA is occasionally difficult distinguish from adenoid cystic carcinoma in terms of clinical and pathological perspectives. An adenoid cystic carcinoma of the parotid gland grows slowly but spreads persistently to the surrounding tissues, particularly along the perineural spaces. In the present case, BCA of the parotid gland was misdiagnosed as an adenoid cystic carcinoma. We discuss the reason for such a misdiagnosis, and present a method for making a correct diagnosis.