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Lymphangioma Circumscriptum in an Adult: An Unusual Oral Presentation
Address for correspondence: Dr. C. Ganesh, No. 28, Ponni Amman Koil Street, Alandur, Chennai - 600 016, Tamil Nadu, India. E-mail: drganesh921@gmail.com
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Abstract
Lymphangioma is a benign hamartomatous tumor of lymphatic vessels. This lymphatic malformation is characterized by an abnormal proliferation of lymphatic vessels. Extra-oral lymphangiomas occur more frequently in the neck region predominantly in the posterior triangle, while intra-oral lymphangiomas are commonly seen in the tongue mainly on the dorsum surface. Various imaging modalities such as ultrasound and color Doppler are very useful in viewing the extent of the lesion. In most of the cases, surgical excision is the treatment of choice. The prognosis is good for most patients, but recurrence has also been reported in some cases, presumably because the lesion is interwoven between muscle fibers, preventing complete removal. This case report discusses the clinical features, color Doppler imaging, histopathology, and treatment of lymphangioma.
Keywords
Color Doppler
lymph vessels
lymphangioma
INTRODUCTION
Lymphangioma is a benign hamartomatous tumor of lymphatic vessels.[1] Described for the first time by Redenbacher in 1828, currently the lymphangiomas are classified as malformations and not as neoplasms.[2] Lymphangioma circumscriptum is usually seen in the extremities and genitals.[3] Lymphangioma is observed after birth or manifests before 2 years of age; consequently, diagnosis for these lesions is rarely performed in adult patients.[4] This case report of lymphangioma circumscriptum, had a very rare site of occurrence in the tongue and the lesion developed in an older patient.
A 29-year-old female patient reported to the Department of Oral medicine and Radiology with a complaint of growth on the right side of the tongue that had developed 17 years earlier. According to the patient, hyperplastic growth was observed on the dorsum surface of the right side of tongue at the age of 12 years but was left untreated. The lesion was initially small and gradually increased to the present size in the next 5-6 years and involved the entire dorsal surface of the tongue on the right side and had remained stable since then. The patient was moderately built and vital signs were within normal limits and there were no visible sins of distress at the time of examination.
On intra-oral inspection, a single, localized, sessile lesion was seen on the right dorsum of the tongue [Figure 1]. The growth measured about 4.5 cm anteroposteriorly, 3.1 cm mesiolaterally and extended 1 mm from the tip of tongue anteriorly and 2 cm in front of sulcus terminalis posteriorly, medially from the midline of the tongue and laterally extended to the lateral borders of the tongue [Figure 2]. Mucosa over the tongue was well-defined reddish in color with a small area of purplish hue seen on the lateral borders of the tongue and had a pebbly surface [Figure 1]. On palpation, it was soft to firm in consistency, mildly tender, pebbly surface, edges were well-defined, with normal surrounding structure. Diascopy, a technique for examining blanching ability of erythematous skin lesions was performed by applying pressure on the lesion with a finger or glass slide and observing change in color of the skin. This test is used to determine if a lesion is vascular or nonvascular or hemorrhagic. Hemorrhagic lesions and nonvascular lesions do not blanch, but vascular lesions blanch. The diascopy test performed on the lesion showed blanching, which suggested it to be a vascular lesion [Figure 3].
RADIOLOGIC FEATURES
Soft-tissue ultrasonograph of the tongue demonstrated a well-defined heterogeneous soft-tissue mass of 2.3 cm × 3.3 cm × 2.4 cm on the right half of the tongue [Figure 4]. Dilated arteries and veins were seen in the right submental region on color Doppler studies suggesting that it could be a vascular malformation [Figure 5].
PATHOLOGIC FEATURES
Incisional biopsy under local anesthesia was performed on the dorsal surface of the tongue and the tissue specimen was sent for histopathological examination. Microscopic section revealed tongue mucosa with marked irregular acanthosis and papillomatosis with thin elongated rete pegs. Adjacent subepithelial tissue showed cavernous vascular spaces lined by flattened epithelium. Deep submucosa showed diffuse chronic inflammation. Deep muscle layer appeared normal suggestive of “lymphangioma circumscriptus” [Figure 6]. Patient was referred to the Department of oral and maxillofacial surgery for further treatment.
DISCUSSION
Lymphangiomas are hamartomatous, congenital malformations of the lymphatic system.[5] They are believed to arise from lymph sac sequestration and enlarge due to inadequate drainage, from lack of communication with the central lymphatic channels or excessive secretion of lining cells.[6]
Lymphangioma is observed on birth or manifests before 2 years of age. In the case reported here, the lesion developed in a patient older than the common age group. The patient was 29-years old at the time of diagnosis and had reported that the problem had persisted for 17 years.[4]
Lymphangioma have a marked predilection for the head and neck region, which accounts for about 75% of all cases.[1] Lymphangiomas have been classified into:
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Lymphangioma simplex (capillary lymphangioma) consists of small, capillary-sized vessels
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Cavernous lymphangioma is composed of large, dilated lymphatic vessels
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Cystic lymphangioma (cystic hygroma) exhibits large macroscopic cystic spaces.[7]
This is also classified according to the clinical presentation into macrocystic (cavities larger than about 2 cm3), microcystic (cavities smaller than about 2 cm3) and mixed, combining these two types.[8]
Oral lymphangiomas occur at various sites, but are most frequently found on the anterior two-thirds of the tongue, where they often result in macroglossia.[1] The lesion can also present in the palate, buccal mucosa, gingival, and lips.[7] Uncommon occurences involve the soft palate and retromolar region.[9] Clinically, the lesions present superficially as a pebbly, vesicle-like feature with so-called “frog-egg” or “tapioca-pudding” appearance. Deeper tumors present as soft, ill-defined masses.[1]
The diagnosis of lymphangiomas is not difficult, being mainly clinical. In lesions with atypical clinical features, a definitive diagnosis should be made through biopsy and histopathological examination, along with imaging studies which are very useful in confirming the diagnosis.[2] Imaging modalities, especially color Doppler can identify the vascular malformation in cases of lymphangioma circumscriptum. Vascular malformations do not contain hyperplastic cells but consist of progressively enlarging aberrant and ectatic vessels composed of a particular vascular architecture such as veins, lymphatic vessels, venules, capillaries, arteries, or mixed vessel types. Vascular malformations are appropriately named by their predominant vessel type (e.g., venous malformations, arteriovenous malformations).[10] In this case it was due to lymphatic vessels and hence it is termed as lymphatic malformation.
The histopathology of lymphangioma circumscriptum is characterized by solitary and grouped dilated cystic spaces in the papillary derma. The cystic spaces are lined by endothelial cells often containing red blood cells, as well as lymphatic fluid. In the deep derma and subcutaneous fat, dilated lymphatic vessels are also seen, some of it containing thickened muscular walls.[2] In this case, histological study showed irregular acanthosis and papillomatosis with thin elongated rete pegs. Adjacent subepithelial tissue showed cavernous vascular spaces lined by flattened epithelium. Deep submucosa shows diffuse chronic inflammation. Deep muscle layer appear normal suggestive of “lymphangioma circumscriptus.”
The objectives of treatment of lymphangiomatous macroglossia are preservation of taste, restoration of tongue size for articulation, correction of mandibular and dental deformities and cosmesis, which in turn are treated using different treatment modalities such as surgical excision, radiation therapy, cryotherapy, electrocautery, sclerotherapy, steroid administration, embolization and ligation, laser surgery and radiofrequency tissue ablation technique. Among these treatment modalities, surgical excision continues to be integral to management in many cases.[5]
CONCLUSION
Although rarely encountered in the oral cavity, lymphangiomas represent a condition that must be recognized. Their early recognition allows proper initiation of treatment and prevents the occurrence of the complications. Color Doppler imaging definitely helps to identify the increased vascularity seen in lymphangioma circumscriptum and also the extent of the lesion, which is essential in optimizing surgical and other treatment modalities.
ACKNOWLEDGMENT
The authors would like to acknowledge Dr. N. Gnansundaram, Former Professor and Head, Department of Oral Medicine and Principal, Tamil Nadu Government Dental college, India for his valuable suggestions and to the Department of Oral Medicine and Radiology, Saveetha Dental College and Hospital, Chennai, India.
Available FREE in open access from: http://www.clinicalimagingscience.org/text.asp?2013/3/1/44/120779
Source of Support: Nil
Conflict of Interest: None declared.
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