Tumor desmoplásico de células redondas / Desmoplastic round cell tumor

Resumen El tumor desmoplásico de células pequeñas y redon das es una neoplasia poco frecuente y muy agresiva que forma parte de la familia de los "tumores de célu las pequeñas, redondas y azules". Presenta una mayor incidencia en el sexo masculino en la segunda década de la vida. Se debe a la translocación t(11;22) (p13;q12). Se puede localizar tanto en el abdomen como en el re troperitoneo caracterizándose por presentar síntomas inespecíficos. El tratamiento es muy variado y no se ha detectado todavía aquel que garantice la cura total del paciente. El objetivo del presente estudio es exponer un caso clínico de tumor desmoplásico como enfermedad abdo minal infrecuente y su expresión imagenológica.

Abstract Desmoplastic small round cell tumor is a rare and very aggressive neoplasm that belongs to the family of "small round blue cell tumors". It has a higher incidence in males in the second decade of life. It is due to trans location t(11;22) (p13;q12). It can be located both in the abdomen and in the retroperitoneum and is character ized by nonspecific symptoms. The treatment is very varied and the one that guarantees the total cure of the patient has not yet been detected. The objective of this study is to expose a clinical case of desmoplastic tumor as an rare abdominal disease and its imaging expression.

A Rare Case Of Retroperitoneal Mature Cystic Teratoma In A Young Male Patient

Retroperitoneal mature cystic teratomas are exceedingly uncommon in young male. They are more common in infants and in young females. We report an unusual case of 27 year old male presented with abdominal distension, abdominal fullness and vomiting. Patient underwent ultrasonography and contrast enhanced computed tomography (CT) scan of abdomen which were suggestive of large mature cystic lesion. Patient was planned for surgery and laprotomy was done. A huge retroperitoneal mass was observed and was totally excised. Onhisto-pathological examination (HPE) stratified squamous epithelium with keratin flakes, underlying fibromuscular tissue reveal hair shaft & sebaceous glands and mature cystic teratomawas diagnosed. Retroperitoneal mature cystic teratoma in an older maleis extremely rare. Primary gonadal teratoma with retroperitoneal metastasis should be excluded first. Evaluation of age and location of tumor are critical for its prognosis.

Leiomiosarcoma retroperitoneal con resección de vena cava / Retroperitoneal leiomyosarcoma with resection of the vena cava

RESUMEN El leiomiosarcoma vascular es un tumor maligno de baja incidencia cuya localización más frecuente es la vena vava inferior (VCI). Se presenta habitualmente en la 6a década de la vida. Según su localización se describen 3 tipos de acuerdo con su relación con las venas suprahepáticas y renales. Los cuadros clínicos de presentación son inespecíficos, ya que suelen debutar como hallazgos o con síndromes de congestión venosa pélvica/miembros inferiores. Su tratamiento quirúrgico radical requiere un equipo multidisciplinario entrenado en cirugía retrope ritoneal y vascular.

ABSTRACT Vascular leiomyosarcomas are rare tumors and are usually localized in the inferior vena cava (IVC). They usually occur in the 6th decade of life. They are classified into 3 groups according to the relation with the hepatic and renal veins. The clinical presentation is unspecific, ranging from an incidental finding to symptoms of venous pelvis congestion of lower extremity edema. Radical resection is the treatment of choice and requires multidisciplinary team trained in retroperitoneal and vascular surgery.

Extra-visceral retroperitoneal echinococcosis: case series with follow-up / Echinococosis retroperitoneal extra-visceral: serie de casos con seguimiento

SUMMARY: Extra-visceral retroperitoneal echinococcosis (EVRE), represents an infrequent condition, even in endemic areas. Its best treatment option is surgery. The aim of this study was to determine postoperative morbidity (POM) and recurrence in patients with EVRE, surgically treated. Case series with follow-up of patients with EVRE undergoing surgery consecutively at RedSalud Mayor Temuco Clinic, between 2008 and 2019. The outcome variables were POM and recurrence. Other variables of interest were cyst diameter, surgical time, and hospital stay. Descriptive statistics was used. In this study, 12 patients (75.0 % male), with a median age of 46 years, were treated. The 58.3 % of cases were primary retroperitoneal cysts. The median of cyst diameter, surgical time, and hospital stay were 15 cm, 95 min, and 4 days respectively. The most frequent type of resection was total cystectomy (58.3 %). MPO was 8.3 % (there was urinary infection in one patient). No reoperations were necessary. There was no operative mortality. With a median follow-up of 90 months, a recurrence of 8.3 % was verified (one case). The results achieved, in terms of POM and recurrence were similar to other series.

RESUMEN: La equinococosis retroperitoneal extravisceral (EREV), representa una condición poco frecuente, incluso en áreas endémicas. Su mejor opción de tratamiento es la cirugía. El objetivo de este estudio fue determinar morbilidad postoperatoria (MOP) y recurrencia de pacientes con EREV tratados quirúrgicamente. Serie de casos con seguimiento de pacientes con EREV intervenidos de forma consecutiva en Clínica RedSalud Mayor Temuco, entre 2008 y 2019. Las variables resultado fueron POM y recurrencia. Otras variables de interés fueron diámetro del quiste, tiempo quirúrgico y estancia hospitalaria. Se utilizó estadística descriptiva. Se trató a 12 pacientes (75,0 % hombres), con una mediana de edad de 46 años. El 58,3 % de los casos fueron quistes retroperitoneales primarios. La mediana del diámetro del quiste, tiempo quirúrgico y estancia hospitalaria fueron 15 cm, 95 min y 4 días, respectivamente. El tipo de resección más frecuente fue la quistectomía total (58,3 %). La MPO fue 8,3 % (infección urinaria en un paciente). No hubo reintervenciones ni mortalidad operatoria. Con una mediana de seguimiento de 90 meses, se verificó una recurrencia de 8,3 % (un caso). Los resultados obtenidos, en cuanto a MPO y recurrencia, son similares a otras series.

Neoplasia endocrina múltiple IIA: feocromocitoma bilateral. A propósito de un caso y revisión de la literatura / Multiple Endocrine Neoplasia IIA: Bilateral Pheochromocytoma. About a Case and Literature Review

Resumen: Presentamos el caso de una paciente del sexo femenino, de 54 años de edad, con antecedente familiar de neoplasia endocrina múltiple tipo II, con estudio genético positivo para NEM 2 IIA EXON 11, c634 CGCIB. Inició padecimiento con cardiopatía hipertensiva y disfunción diastólica, hallazgo to mográfico de tumor suprarrenal bilateral por imagenología, se realizó adrenalectomía convencional transabdominal, se encontró tumor derecho con cápsula correspondiente a feo cromocitoma con un peso de 1,100 g de 14.5 cm de diámetro mayor con invasión a cápsula sin romperla, tumor suprarrenal izquierdo correspondiente a feocromocitoma con un peso de 950 g de 15 cm de diámetro mayor.

Abstract: We present the case of a 54-year-old female patient with a family history of multiple endocrine neoplasia type II, with a genetic study for MEN 2 IIA EXON 11, CG6B c634, onset with hypertensive heart disease and diastolic dysfunction, tomographic finding of bilateral adrenal tumor by imaging. A conventional transabdominal adrenalectomy was performed, finding a right tumor with a capsule corresponding to pheochromocytoma with a weight of 1,100 g of 14.5 cm of greater diameter with invasion of the capsule without breaking it, and a left adrenal tumor corresponding to pheochromocytoma with a weight of 950 g of 15 cm of greater diameter.

A case of retroperitoneal schwannoma

Schwannoma are benign tumours of nerve sheath. They are also called as neurilemmoma. They are rare tumours arising from peripheral nerves, though they can occur anywhere on the body. Schwannoma can arise from any peripheral nerves or spinal nerves. Since they arise from nerve sheath forming schwannoma cells, they are never seen in brain or spinal cord. Schwannoma are often associated with neurofibromatosis-2, schwannomatosis and Carney complex where it is inherited in an autosomal dominant manner. They care often asymptomatic and diagnosed incidentally. Symptoms of schwannoma are related to pressure effects over the surrounding structures, such as limb pain, tingling and numbness, deafness and facial weakness as in vestibular schwannoma. However, most schwannoma are detected incidentally as in the case reported below. A 48 years female was diagnosed with an asymptomatic left para renal lump, which was later confirmed to be a retroperitoneal schwannoma. The patient had no complaints with respect to the lump. The patient underwent a successful surgical excision and had an uneventful recovery.

Calcifying fibrous tumour: a rare case report of an exceptional lesion localized in retroperitoneum, mesentery and pelvis

Calcifying fibrous tumours are rare benign lesions affecting mostly children and young adults. A 17-year-old female presented with abdominal pain and abdominal distention. Physical examination revealed intra-abdominal mass occupying retro peritoneum and right iliac fossa. Excisional biopsy from peritoneum and mesentery were performed. Histopathologically, it was composed of hypocellular hyalinised collagenized stroma, spindle cells, psammomatous and dystrophic calcification and mononuclear inflammatory cell infiltration. Authors are here in reporting a case of calcifying fibrous tumour and discussing its clinical and morphological features with regard to the literature.

Primary retroperitoneum mucinous cystadenoma

Primary retroperitoneal mucinous cystadenomas (PRMCs) are observed more frequently in women with no specific symptoms. A 35 Years old female patient presented with Intermittent abdominal pain in her left flank associated with fullness in abdomen. CECT confirmed a well-defined smoothly marginated homogenous non-enhancing unilocular cystic lesion in retroperitoneum in left lumbar region, separated from the pancreas, left kidney and ovary. On Laprotomy, the retroperitoneal tumor was completely removed, without spillage of its contents.

Fine Needle Aspiration Cytology of Retroperitoneal Masses Under Radiological Guidance

Introduction: Advances in diagnostic radiologic techniqueshas made Fine needle aspiration cytology more specificespecially in hard to access areas like retroperitoneum.Rapid enlargement of tumors occur before clinical signs andsymptoms develop in retroperitoneal area. Present study wasundertaken to study the utility and efficacy of FNAC in earlydiagnosis of neoplastic and nonneoplastic retroperitonealmasses, to study the cytomorphology and diagnostic accuracyof FNAC with respect to tissue diagnosis wherever possible.Material and methods: Study was done in Indira GandhiGovernment Medical College, Nagpur on 70 patients withdiagnosed retroperitoneal masses on radiology either by CTor USG over a period of 2 years. Appropriate staining wasdone and results were compared to histopathology whereveravailable. No major complications occurred during theprocedure or post procedure period. Results were analysed todetermine sensitivity, specificity, diagnostic efficacy of guidedFNAC.Results: Adequate cellular material was obtained in 66cases to study cytomorphology. 46(65.72%) retroperitonealmasses were malignant. 3(4.28%) were benign while 14(20%)were inflammatory. 3 (4.28%)cases were suspicious formalignancy. Cytology was correlated with histopathologicaldiagnosis in all 39 cases where tissue diagnosis was available.Interpretation: No major complications were seen during theprocedure or post FNAC period. Statistical analysis showedsensitivity, specificity and diagnostic accuracy were 100% inthese cases in the present study.Conclusion: FNAC is advantageous in terms of accuracy,rapidity, safety and convenience if done in close cooperationwith radiologist and clinicians. Performed as an OPDprocedure, diagnosis obtained in 24 hours helps to avoidsurgical laparotomy and numerous preoperative investigationsin advanced and inoperable cases and inflammatory lesions.

MRI Finding of Retroperitoneal Desmoplastic Small Round Cell Tumor with Hepatic Metastasis and Portal Vein Thrombosis: a Case Report

Desmoplastic small round cell tumor (DSRCT) is a rare and aggressive malignancy common in young male patient. Typical imaging features of DSRCT include multiple soft tissue masses in the peritoneal cavity, omentum, or mesentery without an organ of origin. This report presents a rare manifestation of DSRCT revealing a solitary large retroperitoneal mass with hepatic metastasis and malignant portal vein thrombosis in 70-year-old women together with the review of literature. The tumor showed a hemorrhagic and necrotic mass with peripheral portion of T2 hypo-intensity and delayed enhancement that indicated desmoplastic stroma with dense cellularity.

Schwannoma de retroperitoneo asociado a Neurofibromatosis tipo I / Retroperitoneal Schannoma associated to type I neurofibromatosis

RESUMEN Los Schwannomas son tumores de origen neural, corresponden al 1 por ciento de los tumores de retroperitoneo. En la mayoría de las ocasiones, son tumores de comportamiento benigno, encontrando que solo del 5 - 18 por ciento son malignos y aún menos frecuente es que sean de alto grado en su histología. Se trata de una paciente de 46 años de edad sin antecedentes crónico degenerativos. Con diagnóstico conocido de neurofibromatosis tipo I. Inició su padecimiento actual tres años previos a su ingreso en 2013, al presentar artralgia de rodilla derecha la cual se asocia a mialgias de forma ipsilateral. Se le solicitó como apoyo diagnostico una resonancia magnética de columna dorsal y lumbar, en la que se reporta una tumoración en la región del retroperitoneo de lado derecho con medidas de 10 x 17 cm con aparente origen espinal en L2 y L3. A pesar de ser masas de origen neural benignas la mayoría de las veces, no es infrecuente su malignización encontrando una cavidad con estructuras vecinas tomada por el tumor. En estos casos, es de vital importancia el manejo preoperatorio de manera multidisciplinaria tanto en la preparación preoperatoria, así como durante el procedimiento quirúrgico(AU)

ABSTRACT Schwannomas are tumors of neural origin and account for 1 percent of retroperitoneal tumors. In many times, they are benign tumors and just 5 to 8 percent are malignant; high degree is even less frequent in its histology. This is a male patient aged 46 years with no history of chronic degenerative problems and diagnosis of type I neurofibromatosis. The disease appeared three years before his admission to hospital in 2013 because of right knee arthralgia associated to myalgias on the same side. Diagnostic support was requested in terms of performance of magnetic resonance of dorsal and lumbar spine; this test reported the presence of a tumor in the right side of the retroperitoneal region, it measured 10 x 17 cm with apparent spinal origin in L2 and L3. Although they are often masses of benign neural origin, their malignization is not rare. There was a cavity with adjoining structures affected by the tumor. In this type of cases, the preoperative management with multidisciplinary involvement both in the preoperative preparation and during the surgical procedure is of vital importance(AU)

Schwannomas mediastinal y retroperitoneal metacrónicos / Metachronous mediastinal and retroperitoneal schwannomas

Los schwannomas, también llamados neurilemomas, son tumores originados en la vaina de los nervios periféricos. El 45% ocurren en cabeza y cuello, solo el 9% en mediastino y el 0,7-2,7% en retroperitoneo. La multicentricidad es extremadamente rara. Presentamos el caso de un paciente de 30 años que consultó por dolor torácico derecho asociado a derrame pleural, al que se le diagnosticó un schwannoma mediastinal posterior, el cual fue resecado en forma completa por cirugía videoasistida. A los 3 años, vuelve a consultar por dolor en flanco derecho y, al estudiarlo, se constata un nuevo schwannoma de localización retroperitoneal, que se resecó por vía abierta dada su posición retrocava. Describimos la metodología de estudio de esta neoplasia y los hallazgos histopatológicos que demostraron su benignidad. Conclusión: es una patología muy infrecuente pero con excelente pronóstico posoperatorio si la resección quirúrgica es completa.

Schwannomas, also known as neurilemmoma, are neurogenic tumors that arise from the peripheral nerve sheaths. Forty-five percent of schwannomas occur in the head and neck, 9% in the mediastinum and 0.7-2.7% in the retroperitoneum. Multiple shwannomas are extremely rare. We report the case of a 30-year old male patient with chest pain in the right hemithorax associated with pleural effusion due to schwannoma of the posterior mediastinum that was completely resected with video-assisted thoracoscopy. Three years later, he presented pain on the right lumbar region due to a retroperitoneal schwannoma behind the vena cava that was completely removed with open surgery. We describe the tests used to evaluate this tumor and the histopathological findings confirming its benign nature. Conclusion: Schwannoma is a rare condition with excellent postoperative outcome after complete surgical resection.

Tumor fibroso solitario y síndrome Doege-Potter / Solitary fibrous tumor and Doege-Potter syndrome

El tumor fibroso solitario es raro. Si bien su localización más frecuente es la pleura, han sido informados algunos casos de ubicación retroperitoneal. Es difícil diferenciarlo imagenológicamente de otras neoplasias, por lo que casi siempre el diagnóstico es histológico. Dado que los tumores fibrosos solitarios tienen presentaciones clínicas muy diversas, una mejor compresión de la ubicación y sus características imagenológicas ayudaría a abreviar la lista de diagnósticos diferenciales. Comunicamos un tumor fibroso solitario de localización retroperitoneal cuyo diagnóstico fue confirmado por examen histológico.

The solitary fibrous tumor is uncommon. Even though it frequently locates in the pleura, a few cases have been reported in the retroperitoneum. Differentiation from other neoplasms is difficult, and therefore the diagnosis is always attained through histological examination. Although solitary fibrous tumors have variable clinical behaviors, a better comprehension of the location and its imaging characteristics would help to decrease the list of differential diagnoses. We report a solitary fibrous tumor located in the retroperitoneum whose diagnosis was confirmed by histological examination.

Establishment method of a rat model of renal ischemia-reperfusion injury by clamping the bilateral renal pedicles through backside and retroperitoneal incision / 中国比较医学杂志

Objective To explore a method to prepare a model of renal ischemia-reperfusion injury, with mild injury to animals, simple and easy to operate and stable effectiveness. Methods Healthy SD male rats were randomly divided into normal group (group C), sham-operated group (group S) and experimental group (IR group). Rats in the experimental group received a median incision in the middle of the back skin. Through the muscle fascia of each side on the back into the bilateral retroperitoneal space, the bilateral renal pedicles were separated, and closed for 50 min with a mini artery clamp without injury, and then the blood perfusion of the bilateral renal pedicles was resumed by releasing the mini artery clamp. Except that the rats of sham operation group were not blocked the renal pedicle, the rest of the operating steps were consistent with the experimental group. The normal group rats were not treated except for anesthesia. To observe the condition of the rats, serum creatinine (SCr), blood urea nitrogen (BUN) and pathologyical changes in the kidney tissues at 24 h after operating. Results Skin incision was 2. 24 ± 0. 27 cm in the group IR, the right incision of lumbar dorsal fascia and muscle was 1. 36 ± 0. 21 cm, and the left incision was 1. 36 ± 0. 24 cm. The operation time was 3. 30 ± 0. 37 min from incising skin to clamping the bilateral kidney pedicles. The successful rate of model preparation reached 95% in the IR group. Compared with the groups C and S, the levels of SCr and BUN were remarkably increased in the IR group (P ＜0. 01), and renal tubular necrosis scores were also significantly increased (P＜ 0. 05). Conclusions The rat model of renal ischemia-reperfusion injury is established by clamping bilateral renal pedicles via dorsal retroperitoneal incision. This surgical procedure is stable and simple, with a high success rate and small incision, less bleeding, and minimal animal injury.

Ectopic adreocortical adenoma——An uncommon etiology of Cushing's syndrome / 中华内分泌代谢杂志

We report a case of cushing's syndrome caused by ectopic adreocortical adenoma. The patient is a 37 years old woman, she was admitted to our hospital for " 2 years history of hypertension and weakness in both lower extremities for 2 months". Physical examination revealed: blood pressure 160/116 mmHg(1 mmHg＝0.133 kPa), body mass index 27.47 kg/m2, moon-face, increased fat in the neck and back, purple marks on abdominal skin, withⅡdegree edema of both lower extremities. Laboratory examination revealed that serum cortisol levels were elevated, loss of normal circadian rhythm, and serum adrenocorticotropic hormone (ACTH) was suppressed, the level of cortisol could not be suppressed in low dose desamethasone suppression test. Adrenal computed tomography ( CT) revealed a nodule in the right retroperitoneum, compression of the renal hilum, no bilateral adrenal adenoma and hyperplasia were found. This patient was diagnosed as corticotropin-independent Cushing's syndrome unequivocally. The clinical symptoms were relieved after successful laparoscopic retroperitoneum resection of the nodule. Pathological exam confirmed adrenocortical adenoma in ectopic adrenal tissue. Thus, we should consider the ectopic corticosteroid-secreting tumor in the context of corticotropin-independent Cushing's syndrome, especially when the imaging studies of adrenal revealed bilateral adrenal glands were normal or atrophic, which helped to make an appropriate strategy treatment.

Primary Extragastrointestinal Stromal Tumor of Retroperitoneum: Poor Response to Tyrosine Kinase Inhibitor

Gastrointestinal stromal tumors (GIST) are the most common sarcomas arising in the gastrointestinal tract. Stromal tumors arising outside the gastrointestinal tract are known as extragastrointestinal stromal tumors (EGIST). EGISTs may occur in omentum, mesentery, or retroperitoneum and are histologically and immunophenotypically similar to that in GISTs. EGISTs are very rare, so pathogenesis, incidence, and prognosis of EGISTs are not defined yet. In particular, there are a few reported literatures on the treatment of metastatic EGISTs. I report a case of a primary EGIST of the retroperitoneum with lung metastasis surgically removed and treated with tyrosine kinase inhibitor.

Absceso del iliopsoas: Claves para el diagnóstico imagenológico / Iliopsoas abscess: Imaging keys to accurate diagnosis

Resumen: Si bien es infrecuente, el absceso del músculo iliopsoas exhibe una alta tasa de morbilidad y mortalidad. Su diagnóstico es difícil debido a las numerosas etiologías y su variada presentación clínica. Objetivo: Discutir las causas, vías de diseminación, diagnósticos diferenciales y manejo del absceso del iliopsoas, poniendo especial énfasis en el rol de la tomografía computada y la resonancia magnética en su diagnóstico. Conclusión: La evaluación con estudios de imagen es esencial para determinar la complejidad, extensión y origen anatómico de esta patología, parámetros que son fundamentales para determinar el pronóstico y el manejo en este tipo de pacientes.

Abstract: Although rare, iliopsoas abscess has a high rate of morbidly and mortality. Its diagnosis is diffiult given the numerous etiologies and varied clinical presentation. Objective: To discuss the causes, dissemination pathways, differential diagnoses and management of iliopsoas abscess; emphasizing the important role of CT and MR through multiple imaging examples. Conclusion: Imagenological analysis is essential to determine complexity, extention, and anatomical origin of this condition, fundamental parameters in the prognosis and management of these patients.

Application of extra-anatomic prosthesis bypass in the retroperitoneum for the treatment of infected abdominal aortic aneurysms / 中华普通外科杂志

Objective To assess the effectiveness of extra-anatomic prosthesis bypass in the retroperitoneum as a treatment for infected abdominal aortic aneurysms (iAAAs).Methods We retrospectively reviewed the records of 10 consecutive patients diagnosed with iAAAs and treated by an extraanatomic prosthesis bypass in the retroperitoneum over the past 7 years.All 10 patients were regularly followed up by outpatient observation after their discharge.Results Ten patients with iAAAs underwent an extra-anatomic prosthesis bypass in the retroperitoneum and debridement of the infected aneurysm.An emergency operation was performed for one patient who underwent concomitant gastrointestinal procedures for aortoduodenal fistula,the other 9 cases underwent an elective operation after an intravenous antibiotic therapy for 2-4 weeks.All 10 patients were definitely diagnosed by one or more sequential CT scans combining with other methods.All patients had at least a positive preoperative blood culture or intraoperative tissue culture during the perioperative period,including Salmonella in 5 cases,Burkholderia pseudomallei in 3 cases,Escherichia coli in 1 case,Klebsiella pneumoniae in 1 case.All patients were discharged in 4-6 weeks after their operations.Except 1 case who died 16 months after surgery,all other patients were alive and were free from graft infection during the follow-up period.Conclusions The extra-anatomic prosthesis bypass in the retroperitoneum for treating iAAAs are safe and effective.

Primary retroperitoneal mucinous cystadenocarcinoma in a male patient.

Primary retroperitoneal mucinous neoplasms are extremely rare tumors. Less than sixty cases have been reported in international literature until date, with striking female predominance. We report a case of primary mucinous cystadenocarcinoma of the retroperitoneum in a 51‑year‑old male presenting with nonspecific abdominal complaints. This case is being highlighted for its rare occurrence in a male patient.

Giant retroperitoneal myelolipoma: case report and literature review / Mielolipoma gigante em retroperitônio: relato de caso e revisão da literatura

Adrenal myelolipomas are unusual benign tumors with an average age of 60 years at onset, often associated with adrenal gland. A 63-year-old female presenting with abdominal discomfort and a large expanding mass in retroperitoneum occupying the right hemiabdomen, with extrinsic compression of adjacent organs, underwent tumor resection. Macroscopic examination of the surgical specimen showed a large yellowish homogeneous lesion with areas of hemorrhage, covered by a thin fibrous capsule. Microscopic analysis revealed a neoplasm composed of mature adipocytes permeated by hematopoietic tissue. There was residual adrenal cortex around the lesion.

Mielolipomas são tumores benignos pouco comuns, com média de incidência de 60 anos, frequentemente associados à glândula adrenal. Relata-se caso de paciente do sexo feminino de 63 anos que apresentava quadro clínico de desconforto abdominal e volumosa formação expansiva em retroperitônio, ocupando hemiabdômen direito com compressão extrínseca de órgãos adjacentes, sendo submetida à ressecção tumoral. A análise macroscópica da peça cirúrgica mostrou volumosa lesão homogênea amarelada com áreas de hemorragia, recoberta por fina cápsula fibrosa. A análise microscópica revelou neoplasia constituída por adipócitos maduros permeados por tecido hematopoiético, notando-se cortical da suprarrenal residual na periferia da lesão.