Giant primary omental cyst: an unusual cause of pseudoascites and hydrocele in a child.

Abdominal lymphangiomas are benign congenital abnormal dilatation and proliferation of lymphatic spaces primarily seen in children. The wide spectrum of symptoms challenges preoperative diagnoses. We present a rare case of a 2-year-old boy presented to pediatrician with massive abdominal distention and left scrotal swelling since the age of 1½ years.

Nano-fluorescence imaging: advancing lymphatic disease diagnosis and monitoring.

The lymphatic system plays a crucial role in maintaining physiological homeostasis and regulating immune responses. Traditional imaging modalities such as magnetic resonance imaging, computerized tomography, and positron emission tomography have been widely used to diagnose disorders in the lymphatic system, including lymphedema, lymphangioma, lymphatic metastasis, and Castleman disease. Nano-fluorescence technology has distinct advantages-including naked-eye visibility, operational simplicity, portability of the laser, and real-time visibility-and serves as an innovative alternative to traditional imaging techniques.

Pericardial Effusion as a Presentation of Lymphangioleiomyomatosis.

Lymphangioleiomyomatosis (LAM) is a rare, systemic neoplastic disease that primarily affects women of childbearing age. The disease can arise sporadically or in association with tuberous sclerosis. It is characterized by the proliferation of abnormal smooth muscle-like cells, leading to cystic lung destruction, accumulation of chylous fluid, and development of abdominal tumors.

Child Abdominal Distension Due to a Massive Retroperitoneal Lymphangioma: A Cyto-Histopathological and Clinical Correlation.

Lymphangiomas are rare benign tumors that result from lymphatic vessel malformations and/or obstructions commonly on the neck and armpits, being rare in the retroperitoneal space. We report a case of a healthy 25-month-old male with a six-month history of abdominal distension and recurrent episodes of diarrhea who was clinically diagnosed with giardiasis. The complementary evaluation showed a cystic formation occupying the whole abdominal cavity and implanted at the abdominal retroactivity.

Diverse clinical manifestations of acquired vulvar lymphangioma: a report of five cases in Vietnamese women.

Acquired vulvar lymphangioma (AVL) is a rare but important condition that requires prompt diagnosis and appropriate management to alleviate symptoms and prevent complications. AVL can erupt locally as isolated or clustered lesions which range from translucent, fluid-filled vesicles to smooth, flesh-colored papules or nodules that exude serous or crystalline liquid spontaneously or after trauma. Clinically, it can also be asymptomatic.

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Intraperitoneal Cystic Lymphangioma (CL) is a rare benign malformative disease of lymphatic origin, with a wide range of clinical symptoms. Diagnosis is based on imaging tests and confirmed by histology. We here report the case of a 54-year-old woman presenting with chronic abdominal pain, with no effect on general condition.

Cervical Suprahyoid Bronchogenic Cyst - a Very Rare Malformation of Primitive Foregut.

A cervical bronchogenic cyst is a rare embryological anomaly of the primitive foregut, with an exceptionally uncommon occurrence in a suprahyoid location attached to the parotid tail. We report a case of an asymptomatic neck mass initially diagnosed as either a branchial cleft cyst or lymphangioma based on clinic-radiological investigation, which was subsequently confirmed as an ectopic bronchogenic cyst through histopathological examination.

Symptomatic presentation and imaging features of a chylous cystic lymphangioma.

A woman in her 60s presenting with 5 days of diffuse abdominal pain was diagnosed preoperatively with a chylolymphatic mesenteric cyst. MRI and CT imaging demonstrated a 5.8 cm unilocular cyst containing a fluid-fluid level within the mesentery.

Case report: - A case report on adult-onset cystic hygroma and literature review.

Introduction: Cystic hygromas are benign lesions arising due to an abnormality of lymphoid development and rarely present in adults.

Case Presentation: We present a case of a 25-year-old girl who presented with a complaint of left lateral neck swelling of 06 years duration which was painless and increased in size progressively associated with this she had some difficulty turning her neck to the left side of a year duration. On physical examination, it was noticed that she had a 15 ∗ 12 cm soft, non-tender mass over the left lateral neck from the sub-mandibular area to the supraclavicular area, anterior and posterior to the sternocleidomastoid muscle.

Cavernous Lymphangioma of the Neck: An Extraordinary Case.

Cervical lymphangioma is a congenital malformation of the lymphatic system that shows a predilection for the head and neck regions. They are most common in children between the ages of three and five and are rarely present in adults. While over 90% of lymphatic malformations are congenital, they can also manifest later due to factors such as trauma, infection, tumors, or medical procedures.

Giant cystic lymphangioma as a rare cause of acute abdomen in infancy: a case report and literature review.

Lymphangioma, a benign mass of lymphatic origin, primarily affects the head, neck, and oral cavity, with the abdomen being an uncommon location. Clinical presentation is defined by site of origin and size. We present the case of a 10-month-old male infant with no previous medical history, admitted to our department with diffuse abdominal pain and distension.

Cervical thymic cysts in children: A case report.

Introduction And Importance: Cervical thymic cysts are rare benign lesions that rarely considered in the differential diagnosis of neck cysts in children. The correct diagnosis is often made after surgical excision and though determination of the specific histopathological findings of the thymic cyst.

Case Presentation: We report an observation of a cervical thymic cyst erroneously diagnosed preoperatively respectively as a cystic lymphangioma.

A case report of a mesenteric cystic lymphangioma in a young adult woman presenting to the emergency room.

Background: Mesenteric cystic lymphangiomas (MCLs) are rare benign tumours seen in adults. The clinical presentation may vary from asymptomatic to acute abdominal pain with inexplicable abdominal pain, nausea and vomiting.

Case Presentation: In the current case report, a 22-year old, healthy women presented to the emergency room with acute abdominal pain in need of urgent surgical exploration.

Mesenteric cysts.

<b>Introduction:</b> Mesenteric cysts (MCs) are a rare pathology of the abdominal cavity (with an incidence of 1/27.000 to 1/250.000 admissions) and less than 1000 cases have been described in the specialized literature.

The safety and feasibility of laparoscopic partial splenectomy: analysis of perioperative indications from different vascular subtypes and improvement of surgical approach.

Introduction: While laparoscopic splenectomy (LS) has been widely used in benign splenic tumor, more concerns have been raised for postoperatively short-term and long-term complications. Laparoscopic partial splenectomy (LPS) is a surgical option, to preserve splenic function, and reduce postoperative complications. The aim of our study was to retrospectively identify the safety and feasibility of LPS compared with LS in patients with splenic benign tumor.