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1.
Rozhl Chir ; 103(6): 224-227, 2024.
Article in English | MEDLINE | ID: mdl-38991786

ABSTRACT

INTRODUCTION: Lymphangiomas belong to the group of benign vascular tumors that originate in the lymphatic tissue. Up to 90% of cases manifest in children before the second year of life. In adults, their presence is very rare. In most cases, they are located in the head, neck and axilla. Intra-abdominal lymphangiomas are very rare and represent less than 1% of all cases. CASE REPORT: The authors present the case of a 64-year-old female patient diagnosed with an intra-abdominal cystic lesion following a routine examination. A CT scan of the abdomen confirmed a cystic lesion located in the lesser omentum between the left lobe of the liver and the lesser curvature of the stomach. The patient was scheduled for laparoscopic exstirpation of the lesion. Histological examination confirmed the clinical diagnosis of cystic lymphangioma of the lesser omentum. CONCLUSION: The etiopathogenesis of lymphangiomas remains unclear. Despite the fact that they are benign tumors, lymphangiomas tend to have an infiltrative pattern of growth, invading surrounding structures. The majority of cases are asymptomatic and the diagnosis is incidental. The gold standard in treatment remains complete surgical extirpation with microscopically negative margins.


Subject(s)
Lymphangioma, Cystic , Omentum , Peritoneal Neoplasms , Humans , Lymphangioma, Cystic/surgery , Lymphangioma, Cystic/pathology , Lymphangioma, Cystic/diagnosis , Lymphangioma, Cystic/diagnostic imaging , Female , Omentum/pathology , Omentum/surgery , Middle Aged , Peritoneal Neoplasms/pathology , Peritoneal Neoplasms/surgery , Peritoneal Neoplasms/diagnostic imaging , Peritoneal Neoplasms/diagnosis , Tomography, X-Ray Computed
2.
Rozhl Chir ; 102(6): 251-256, 2023.
Article in English | MEDLINE | ID: mdl-38286654

ABSTRACT

Ladd's syndrome is a complex gastrointestinal anomaly that occurs based on congenital intestinal malrotation and leads to midgut volvulus and intestinal obstruction. It is mostly discovered in paediatric patients and presents itself in 90% of cases within the first year of life. It is a rare diagnosis in adult patients. We present the case report of a 19-year-old female patient with chronic abdominal pain and upper-type dyspeptic syndrome. MRI examination of the abdomen showed an abnormal location of the loops of the small intestine predominantly in the right part of the abdomen, caecum and c. ascendens in the epigastrium, duodenojejunal transition compressed and stenotized between upper mesenteric vessels and the aorta, with prestenotic dilatation of the duodenum and stomach and the "whirlpool sign" in mesentery. The patient was indicated for operational procedure and Ladd's operation was successfully performed laparoscopically, where "Ladd's bands" were divided; the procedure also included adhesiolysis, mobilization of the duodenum with its straightening, widening of the base of the mesentery, appendectomy and removal of an incidental solitary mesothelial cyst. A highly differentiated incidental neuroendocrine tumour of the apex of appendix was confirmed by histology. In the discussion, we focus on the rarity of intestinal malrotation in adulthood, clinical manifestation of the disease, diagnostic options and surgical treatment.


Subject(s)
Appendiceal Neoplasms , Appendix , Digestive System Abnormalities , Intestinal Volvulus , Neuroendocrine Tumors , Female , Humans , Young Adult , Intestinal Volvulus/diagnostic imaging , Intestinal Volvulus/surgery , Intestines , Neuroendocrine Tumors/diagnosis , Neuroendocrine Tumors/surgery , Laparoscopy
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