scholarly journals Malignant Peritoneal and Retroperitoneal Neoplasm

2020 ◽  
Author(s):  
Keyword(s):  
Retroperitoneal Neoplasm

Thrombosed interrupted inferior vena cava and retroaortic left renal vein mimicking retroperitoneal neoplasm

2006 ◽  
Vol 32 (3) ◽  
pp. 403-406 ◽  
Author(s):  
Sevdenur Cizginer ◽  
Servet Tatli ◽  
Jeffrey Girshman ◽  
Joshua A. Beckman ◽  
Stuart G. Silverman
Keyword(s):  
Inferior Vena Cava ◽  
Renal Vein ◽  
Inferior Vena ◽  
Left Renal Vein ◽  
Vena Cava ◽  
Retroperitoneal Neoplasm

scholarly journals Ectopic bronchogenic cyst in the retroperitoneal region: a case report and literature review of adult patients

BMC Surgery ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Kaitao Yuan ◽  
Man Shu ◽  
Yan Ma ◽  
Weidong Feng ◽  
Jinning Ye ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Cystic Lesion ◽  
Bronchogenic Cyst ◽  
Intervertebral Disc Herniation ◽  
Lumbar Intervertebral Disc ◽  
Retroperitoneal Neoplasm ◽  
Laparoscopic Excision ◽  
Lumbar Intervertebral Disc Herniation ◽  
Retroperitoneal Bronchogenic Cyst

Abstract Background Bronchogenic cyst is congenital aberration of bronchopulmonary malformation, which is rarely encountered in the abdomen and retroperitoneum. We present a case report and literature review of retroperitoneal bronchogenic cyst. Case presentation A 53-year-old female presented to outpatient clinic for a routine checkup of lumbar intervertebral disc herniation. She received a contrast computed tomography scan of the abdomen which revealed a retroperitoneal cystic lesion below the left crura of diaphragm. Afterward, the patient underwent a laparoscopic excision of the cystic lesion and was discharged uneventfully at postoperative day 4. Histopathological findings confirmed the diagnosis of retroperitoneal bronchogenic cyst. Our literature review identified 55 adult cases in recent two decades. The average age at diagnosis was 43.2 (range 17–69) years. 44 (80%) cases had a retroperitoneal cyst on the left side, and 52 (94.5%) cases underwent curative excision through open or laparoscopic surgery. In the available follow up of cases, there was no recurrence after surgery. Conclusions Bronchogenic cyst is rare in the retroperitoneal region. It should be considered as one of the differential diagnoses of a retroperitoneal neoplasm.

scholarly journals Peritoneal and Retroperitoneal Neoplasm

2020 ◽  
Author(s):  
Keyword(s):  
Retroperitoneal Neoplasm

scholarly journals Radio-pathological correlation of a retroperitoneal teratoma in a 2-year-old girl: a case report

2021 ◽  
Vol 7 (2) ◽  
pp. 28-31
Author(s):  
Deki Choden ◽  
Kinley Sangay Dorji ◽  
Sonam Choden
Keyword(s):  
Case Report ◽  
Surgical Excision ◽  
Abdominal Distension ◽  
Imaging Findings ◽  
Complete Excision ◽  
Palpable Mass ◽  
Retroperitoneal Teratoma ◽  
Retroperitoneal Neoplasm ◽  
Complete Surgical Excision ◽  
Retroperitoneal Tumors

ABSTRACTRetroperitoneal teratoma is a extragonadal germ cell tumor comprising 5% of all teratomas in children, and the third most common retroperitoneal neoplasm in children. This is a case report of a 2 years old girl who presented with abdominal distension and palpable mass. The imaging findings of the mass was characteristic of retroperitoneal teratoma which was confirmed by histopathology report following complete excision. Retroperitoneal tumor is an uncommon tumor in children with characteristic imaging findings. Computed tomography is mainly used to evaluate the extent of the disease. Most of the retroperitoneal tumors are benign and curable with complete surgical excision.

Retroperitoneal Neoplasm

2020 ◽  
Author(s):  
Keyword(s):  
Retroperitoneal Neoplasm

Giant Kidney Worm {Dioctophyma renale) Infection Mimicking Retroperitoneal Neoplasm

1986 ◽  
Vol 10 (7) ◽  
pp. 508-512 ◽  
Author(s):  
Tsieh Sun ◽  
Alan Turnbull ◽  
Philip H. Lieberman
Keyword(s):  
Retroperitoneal Neoplasm

scholarly journals Unicentric Castleman’s Disease Masquerading Pancreatic Neoplasm

2012 ◽  
Vol 2012 ◽  
pp. 1-3
Author(s):  
Saurabh Jain ◽  
Souvik Chatterjee ◽  
Jyoti Ranjan Swain ◽  
Pritha Rakshit ◽  
Partha Chakraborty ◽  
...  
Keyword(s):  
Lymph Nodes ◽  
Male Patient ◽  
Pancreatic Neoplasm ◽  
Castleman’S Disease ◽  
Unknown Etiology ◽  
Published Data ◽  
Castleman's Disease ◽  
Retroperitoneal Neoplasm

Castleman’s disease is a rare nonclonal proliferative disorder of the lymph nodes with an unknown etiology. Common locations of Castleman’s disease are mediastinum, neck, axilla, and abdomen. Castleman’s disease of a peripancreatic location masquerading as pancreatic neoplasm is an even rarer entity. On search of published data, we came across about 17 cases published on peripancreatic Castleman’s disease until now. Here we are reporting a case of retropancreatic Castleman's disease masquerading as retroperitoneal neoplasm in a 46-year-old male patient.

scholarly journals Multiple Myeloma in the Practice of a Primary Care Physician: A Clinical Case

2020 ◽  
Vol 27 (3) ◽  
pp. 139-145
Author(s):  
A. E. Shklyaev ◽  
E. A. Semenovikh ◽  
E. S. Gaysina
Keyword(s):  
Primary Care ◽  
Multiple Myeloma ◽  
Primary Care Physician ◽  
Clinical Case ◽  
Abdominal Cavity ◽  
Percutaneous Biopsy ◽  
Care Physician ◽  
Lumbosacral Spine ◽  
Retroperitoneal Neoplasm ◽  
The Right

Aim. To demonstrate difficulties in diagnosing multiple myeloma at the out-patient stage on the example of a clinical case.Materials and methods. The course of establishing a diagnosis in a 58-year-old patient complaining of pain in the hip joint was analysed on the basis of the patient’s medical records both at the out-patient and in-patient stages.Results. A case of multiple myeloma occurring under the guise of common degenerative-dystrophic diseases is presented. An oncological diagnosis was suspected due to the patient’s complains of persistent pain, which was poorly relieved by non-steroidal anti-inflammatory pain agents, and progressive changes in the general blood test (acceleration of ESR to 40 mm/h, and then to 50 mm/h; reduction of hemoglobin from 145 g/l to 134 g/l). The diagnostic search started with an ultrasound examination of the abdominal cavity and pelvic organs, which revealed both an extensive formation in the pelvis in the right iliac region and the lymphadenopathy of the inguinal lymph nodes. Subsequently, spiral computed tomography of the abdominal cavity and the pelvis was conducted. In all bones at the study level, multiple spherical solid formations with uneven contours causing destruction of bone tissue were detected, allowing myeloma to be suspected. The patient was referred to the Republican Clinical Oncology Dispensary, where a percutaneous biopsy of the retroperitoneal neoplasm, as well as morphological and immunohistochemical studies, were carried out. As a result, the following diagnosis was established: multiple stage IIIA myeloma, first detected, with damage to the thoracic, lumbosacral spine, ribs, pelvic, and thigh bones. The patient was hospitalised in the Hematology Department of the First Republican Clinical Hospital, where he underwent chemotherapy according to the VCD scheme (bortezomib, dexamethasone, cyclophosphomide), and was discharged with improvement.Conclusion. The diagnosis of multiple myeloma is a challenging task for a primary care physician due to the diversity of the clinical picture and the lack of clinical suspicion. At the same time, timely diagnosis of the disease at the out-patient stage can significantly increase the effectiveness of treatment and, therefore, improve the prognosis. Thus, more attention should be paid to the differential diagnosis of degenerative diseases of the musculoskeletal system and multiple myeloma.

scholarly journals A Brief Study on Retroperitoneal Paraganglioma

2021 ◽  
pp. 64-66
Author(s):  
Milind Pandey ◽  
Sunita Vagha ◽  
Gaurav Mahajan ◽  
Anchal Manchanda
Keyword(s):  
Vascular Malformations ◽  
Abdominal Cavity ◽  
Endocrine Tumors ◽  
Retroperitoneal Neoplasm ◽  
Contrast Enhanced Ct ◽  
Contrast Enhanced ◽  
Enhanced Ct ◽  
Tingling Sensation ◽  
Specific Tissue ◽  
Primary Retroperitoneal

Paragangliomas are tumors of the autonomic nervous system, located extra-adrenally, presenting inside the base of the head, chest and abdomen. They can appear as a primary retroperitoneal neoplasm when viewed inside the abdominal cavity and might resemble as vascular malformations or any other conditions same as retroperitoneal organs particularly such as pancreas, kidney. These are relatively uncommon endocrine tumors that originate from specific tissue of the paraganglion. They synthesise, store and secrete catecholamines, which can contribute to headache, sweating, palpitation and hypertension. These may be mistaken for GISTs with no histological diagnosis and symptoms of catecholamine overload (non functional). We are reporting a case of 42 yrs male with clinical features of slow backache radiating to both lower legs and with the presence of tingling sensation. Corresponding contrast enhanced CT scan shows a para – aortic mass.

Sign in / Sign up

Export Citation Format

Share Document