Cystic lymphangioma of the breast. First case in Russian clinical practice

In this article, we review of the existing literature on cystic lymphangiomas and report a case of cystic lymphangioma of the breast in an 83‑year-old patient. This case required differential diagnosis between infiltrative cancer and cystic lymphangioma of the breast. The patient has undergone surgery (tumor removal). No complications were observed.

Huge Retroperitoneal Lymphangioma Presenting With Duodenal Obstruction: a case report.

lymphangiomas are benign tumors caused by the congenital proliferation of lymphatic tissue, causing an obstruction in the lymphatic ducts, producing fluid filled cysts (1). Histologically they are polycystic, with cysts divided by thin septas lined with endothelial cells. Most common presentation of cystic lymphangiomas are in the neck (75%) and axillary region (20%) and only 5% are intra-abdominal, while retroperitoneal lymphangiomas account for only 1% of cases (2). It is more common in children with males affected more than women, while women have shown to encounter pancreatic lymphangiomas more than men (3). Often retroperitoneal lypmhangiomas are asymptomatic but due to their large size they might cause a wide variety of symptoms from mild abdominal distention/discomfort and back pain to duodenal obstruction, sepsis and DIC (4). Diagnostic techniques are ultrasound, CT scan and MRI but often it is found accidentally and definitive diagnosis is made post-operatively. Treatment of choice is complete surgical resection with cystectomy

Pathological Discrepancy: Simple Mesenteric Cyst vs. Mesenteric Lymphangioma

Introduction. Both mesenteric cysts and cystic lymphangiomas are scarce and clinically and radiologically almost identical derivatives, but their histological structure is fundamentally different. Case Presentation. A 52-year-old woman was consulted by a surgeon for a derivative felt in her abdomen. The patient said she felt a growing derivative in the abdomen about a month ago. After consulting and testing, a sigmoid colon mesenteric cyst ( 13 cm × 11 cm × 10 cm ) was found. Complete excision of the cyst within healthy tissues was performed through laparotomy. The surgery had no complications. The initial pathological answer was a simple mesothelial cyst (a rare histological finding). However, immunohistochemical tests were performed that showed that diagnosis was mesenteric cystic lymphangioma (ML). Cystic lymphangiomas that have a link to the mesentery have been described less than 200 times. Conclusions. Final differential diagnosis between different cystic derivatives is possible only based on histopathological examinations. Mesenteric lymphangioma is most common at a very young age, but in rare cases, it also occurs in adults. All clinicians should increase their awareness of the disease.

Cystic Lymphangioma: A Rare Cause of Haemorrhagic Ascites

Lymphangiomas are congenital malformations of the lymphatic system. Multiple intra-abdominal cystic lymphangiomas are rare in adults. Author present a case of a 39-year-old male, presenting with recurrent episodes of haemorrhagic ascites. Laparoscopic biopsy and imaging investigations revealed multiple intra-abdominal cystic lymphangiomas involving the spleen, the liver and the retro-peritoneum. Surgical excision including splenectomy, excision of retroperitoneal and mesenteric lesions was done. The patient has been asymptomatic for 2 years on follow-up.

Cystic lymphangioma of abdominal wall in an adult,Rare site of occurance

Cystic lymphangiomas are rare, congenital, benign lesions occurring early in life, mainly in the head, neck, and oral cavity and rarely in abdominal wall, Due to aberrant proliferation of lymphatic vessels resulting from abnormal development of the lymphatic system. Lymphangiomas are classified as micro cystic, macro cystic, and cystic hygromas according to the size of the lymphatic cavities incorporated. These are soft, variable in size and shape, and tend to grow extensively if not surgically excised. These are multilocular cysts filled with clear or yellow lymph fluid. Histopathologically, lymphangiomas are of three types: Lymphangioma simplex, Cavernous Lymphangioma, and Cystic Hygroma depending on the size of vascular spaces and thickness of the adventitia. The present case report describes a case of cystic lymphangioma of lower abdominal wall in a 30-year-old male and its clinical, ultrasonographic / Imaging features, cytological and histopathological correlation.

Doxycycline Sclerotherapy of a Cervical Cystic Hygroma: A Caribbean Institution Experience

Cervical cystic lymphangiomas are rare benign tumors that pose a formidable challenge to surgeons confronted with managing this uncommon entity. Due to the intimacy with which these cystic lesions blend with critical cervical structures, a considerable number of patients who undergo surgical management are often plagued with recurrence and morbidity. As a result, doxycycline sclerotherapy has become an attractive, safe, and effective alternative as a primary treatment modality in a select group of pediatric patients. This case report presents an 18-month-old patient with a large cervical cystic hygroma that was effectively treated with exclusive doxycycline sclerotherapy.

Cystic lymphangioma of abdominal wall in an adult: a rare site

Cystic lymphangiomas are rare, congenital, benign lesions occurring early in life, mainly in the head, neck, and oral cavity, rarely occur in abdominal wall and its discovery in adult is also very rare. It is due to aberrant proliferation of lymphatic vessels resulting from abnormal development of the lymphatic system. These are soft, variable in size and shape and tend to grow extensively if not surgically excised. These are multilocular cysts filled with clear or yellow lymph fluid, sometime mixed with blood. The present case report describes a case of cystic lymphangioma of right lower abdominal wall in a 36 years old male and its clinical, ultrasonographic, CECT, and histopathological correlation.

Cystic lymphangioma of the stomach with marked reactive changes: a rare cause of gastric outlet obstruction in adult

Cystic lymphangiomas are benign lymphatic tumours which usually affect the paediatric population and are predominantly located in the head and neck region. Its occurrence during adulthood and an intra-abdominal location are both extremely uncommon. Clinically and radiologically, these lesions often mimic malignancy. Infrequently, these tumours can undergo degenerative and reactive changes obscuring the diagnostic features. We describe hereby an anecdote of cystic lymphangioma with marked reactive changes presenting with the features of gastric outlet obstruction in an adult patient.