Neonatal Ovarian Lymphangioma

Jallouli, Mohamed; Trigui, L.; Gouiaa, Naourez; Gargouri, Abdellatif; Mhiri, Riadh

doi:10.1016/j.jpag.2010.08.008

Cited by 9 publications

(3 citation statements)

References 5 publications

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“…The lymphatic system comprises unidirectional lymphatic vascular channels that transport lymph toward the subclavian vein [ 4 ]. Lymphangiomas are rare and benign lesions that most often occur in the head, axillary region and neck.…”

Section: Discussionmentioning

confidence: 99%

Ovarian Cystic Lymphangioma

Sharma,

Raghuvanshi,

Kumar

et al. 2024

Cureus

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Lymphangioma are benign, slow-growing and rare lymphatic tumors, which may emerge at any location in the body with ovary being a very rare location. Axillary region and neck are the most common sites, while retroperitoneum and mesentery account for <1%. We present a case of a young female of 33 years who had symptomatic pelvic mass and was presented with a complaint of lower abdominal pain of six-month duration and weight loss. Investigation revealed an oval-shaped complex cystic density lesion in the right adnexal region, which was likely neoplastic. Elective laparotomy with right ovarian cystectomy was performed. Histopathological examination revealed ovarian lymphangioma.

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Section: Discussionmentioning

confidence: 99%

Ovarian Cystic Lymphangioma

Sharma,

Raghuvanshi,

Kumar

et al. 2024

Cureus

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“…The lymphatic system comprises of a network of uni-directional lymphatic vessels that carry clear fluid called lymph directed towards the heart [5]. The lymphatic vessels are found throughout the body sparing the brain, anterior chamber of the eye and in organs composed of rich sinusoidal networks such as bone marrow and spleen.…”

Section: Discussionmentioning

confidence: 99%

Ovarian Cystic Lymphangioma: A Rare Case Report with Review of Literature

Narla¹,

Arshee²,

Kurian³

2020

Int J Pathol Clin Res

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Lymphangiomas of the ovary are unusual benign tumours characterised by proliferation of lymphatic channels, composed of cystic spaces lined by a single layer of endothelial cells. We present a case of 61-year-old woman who presented with complaints of pain abdomen. Investigations revealed a large left ovarian multiseptate multiloculated cystic mass extending to pelvis, abdominal cavity and infraumbilical region likely neoplastic. Total abdominal hysterectomy with bilateral salpingo-oophorectomy was performed suspecting malignancy. Histopathological examination revealed an ovarian lymphangioma. Patient was disease free 1 year post-surgery. Ovarian cystic lymphangiomas must be included in the differential diagnosis of cystic ovarian masses and long term follow up is suggested to exclude a possibility of malignant transformation.

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“…Some cases have been described in neonates and children. [7,8] Owing to the paucity of cases, their exact incidence and malignant potential is not well known. They are usually benign, and only two cases with malignant transformation were found to have been reported to date.…”

Section: Discussionmentioning

confidence: 99%

A rare case of ovarian lymphangioma with elevated CA-125 causing pseudo-Meigs’ syndrome

et al. 2019

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Lymphangiomas are benign congenital malformations of the lymphatic system, thought to occur as a result of obstruction of the local lymph flow system. They can occur anywhere in the skin and mucous membranes. The most common sites are the head and neck, but sometimes they are found in the intestines, pancreas and mesentery. Lymphangioma of the ovary is an extremely rare lesion. It was first described in 1908. Clinical manifestations can vary, from an asymptomatic ovarian mass to an acute abdomen. These may be confused with malignant ovarian masses, resulting in extensive surgery. A 34-year-old woman presented with dull aching pain localised to the lower abdomen, present for the previous 6 months. Ultrasound and a contrast-enhanced computed tomography scan of the abdomen were suggestive of an enlarged right ovary with massive ascites. The cancer antigen 125 (CA-125) level was 685 units/mL. Diagnostic laparoscopy revealed chylous ascites, and further, a frozen section revealed a few atypical cells, additionally strengthening the diagnosis of a malignant tumour. Staging laparotomy with total abdominal hysterectomy and salpingo-oophorectomy was finally performed. Histopathology revealed lymphangioma, with no evidence of malignancy. CA-125 also showed a rapid decline following surgery. Lymphangiomas should be included in the differential diagnosis of ovarian cystic masses, especially in patients with chylous ascites. It is very important to discriminate such cases from other malignant tumours in order to avoid overtreatment. However, a careful follow-up for at least 2 years is needed for patients with lymphangioma of the ovary, to exclude recurrence.

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Neonatal Ovarian Lymphangioma

Cited by 9 publications

References 5 publications

Ovarian Cystic Lymphangioma

Ovarian Cystic Lymphangioma

Ovarian Cystic Lymphangioma: A Rare Case Report with Review of Literature

A rare case of ovarian lymphangioma with elevated CA-125 causing pseudo-Meigs’ syndrome

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