Paniculitis epiploica aislada en un niño con dolor abdominal: A propósito de un caso / Isolated omental panniculitis in a child with abdominal pain: Case report

La paniculitis epiploica aislada es una entidad rara, mayormente observada en los adultos. Se presenta con inflamación del tejido adiposo del epiplón. Los síntomas varían entre manifestaciones locales (por ejemplo, dolor a la palpación abdominal o una masa palpable) y sistémicas, que incluyen dolor abdominal, dolor de espalda, fiebre, descenso de peso y trastornos intestinales. Presentamos este caso como una primera acción de sensibilización respecto de un caso de paniculitis epiploica en un niño, afección que debe tenerse en cuenta en el diagnóstico diferencial del íleo a fin de evitar cirugías innecesarias.

Isolated omental panniculitis is a rare entity mostly seen in adults. It presents with the inflammation of the fatty tissue of the omentum. The symptoms may vary from local (e.g. abdominal tenderness or palpable mass) to systemic manifestations including abdominal pain, back pain, fever, weight loss and bowel disturbances. We presented this case as a first awareness of omental panniculitis in a child which must be kept in mind at the differential diagnosis of ileus so that unnecessary surgeries might be avoided.

Paniculitis mesentérica asociada a enfermedad relacionada con IgG4 como causa de fiebre de origen desconocido / Mesenteric panniculitis associated with IgG4-related disease as a cause of fever of unknown origin

La paniculitis mesentérica es un raro desorden inflamatorio de la grasa mesentérica, de la cual hay, hasta ahora, aproximadamente 200 casos reportados en la literatura. Se presenta en adultos a partir de la tercera década de la vida y su etiología es desconocida, pero es sabida su asociación con neoplasias gastrointestinales, genitourinarias y enfermedades reumatológicas. Entre sus manifestaciones clínicas están el dolor abdominal, las alteraciones del tránsito intestinal, la pérdida de peso, la fiebre y los vómitos. El diagnóstico definitivo es fundamentalmente histopatológico, también existen algunos estigmas tomográficos que podrían sugerir su presencia. Debe ser tratada a la mayor brevedad posible y los corticosteroides son los medicamentos a elegir. Se presentó un paciente con diagnóstico de paniculitis mesentérica idiopática, como resultado del estudio de una fiebre de origen desconocido, en el cual logramos además demostrar la asociación de la paniculitis con la enfermedad relacionada con IgG4, desorden recientemente descubierto, caracterizado por lesiones inflamatorias seudotumorales, que cursan con infiltración hística por células plasmáticas IgG4 positivas.

Mesenteric panniculitis is a rare inflammatory disorder of the mesenteric fat, of which there is, so far, about 200 cases reported in the literature. It occurs in elderly adults and its etiology is unknown but its association with gastrointestinal tumors, genitourinary and rheumatological diseases is known. Among its clinical manifestations are abdominal pain, altered bowel movements, weight loss, fever and vomiting. The definitive histopathological diagnosis is fundamentally, there is some tomographic stigma that might suggest its presence. It should be treated as soon as possible and corticosteroids are the drugs of choice. A patient diagnosed with idiopathic mesenteric panniculitis as a result of the evaluation of fever of unknown origin, which we further demonstrate the association of panniculitis with related disease IgG4, disorder recently discovered, characterized by lesions in flammatory pseudotumoral occurs, that occur with tissue infiltration IgG4 positive plasma cells.

A Case of IgG4-Related Sclerosing Mesenteritis Associated with Crohn's Disease / 대한소화기학회지

Sclerosing mesenteritis (SM) is a rare disease characterized by chronic nonspecific mesenteric inflammation and fibrosis of unknown etiology. Some tumefactive SM shows diffuse accumulation of IgG4-positive plasma cells and is considered as a part of the spectrum of IgG4-related disease. An association between inflammatory bowel disease and IgG4-related disease has been indicated. A 45-year-old woman visited our hospital due to weight loss with intermittent lower abdominal discomfort. Pelvic ultrasound revealed a mass-like lesion in the abdominal wall and pelvis MRI demonstrated a 5.9 cm sized wall-enhancing mass with heterogeneous signal intensity from right adnexa to the abdominal wall. Tumor resection and adhesiolysis was done because of severe adhesion with the small bowel, colon, bladder, uterus, and abdominal wall. Appendectomy was also performed due to adhesion and edematous change. Histological examination of the resected mass showed findings that were compatible with IgG4-related SM. The resected appendix showed chronic granulomatous inflammation without evidence of tuberculosis. She was diagnosed with Crohn's disease after undergoing colonoscopy and CT enterography. Herein, we report a rare case of IgG4-related SM that occurred in conjunction with Crohn's disease.

Appropriate Administration Timing and Clinical Indications of Thiopurine in Crohn's Disease / 대한소화기학회지

No abstract available.

Efficacy of colchicine in the treatment of mesenteric panniculitis in a young patient

Mesenteric panniculitis [MP] is a rare inflammatory and fibrotic disease of the mesentery of unknown etiology. It has various clinical and radiological manifestations, posing a diagnostic challenge for clinicians. Its diagnosis is indicated via radiologic imaging and is usually confirmed via peritoneal biopsies. We describe a case of a patient with histopathologically proven MP, in which steroid dependence was successfully managed with colchicines

Spontaneous Regression of Sclerosing Mesenteritis Presenting as a Huge Mass / 대한소화기학회지

Sclerosing mesenteritis is a rare benign disease originated from the mesenteries. It can be related to autoimmune disease, vasculitis, ischemia, infection, trauma and operation, but most of cases are idiopathic. The overall prognosis of sclerosing mesenteritis is usually good with benign, course. However, no consensus of treatment has yet been established. We report a case of spontaneous partial regression of sclerosing mesenteritis presented as a huge mass and diagnosed by finding of contrast enhanced abdominal computed tomography and percutaneous ultrasonography guided needle biopsy.

Paniculitis mesentérica asociada con absceso intraabdominal / Mesenteric panniculitis with intraabdominal abcess: report of one case

La paniculitis mesentérica es una enfermedad inflamatoria del tejido adiposo del mesenterio, de presentación infrecuente y que se caracteriza, por el engrasamiento, endurecimiento y nodularidad del mismo. Se pone en consideración un caso clínico en un varón joven, con una forma de presentación poco común que requirió de laparotomía exploradora para realizar el diagnóstico y tratamiento.

We report a 28 years old obese male presenting with abdominal pain of increasing intensity lasting 15 days. In the last days, diarrhea and fever appeared. On abdominal examination a 8 cm painful mass was palpated. An abdominal ultrasound showed an anechoic mass in the epigastrium. An abdominal CAT sean showed an inflammatory mass that involves the small bowel. The patient is subjected to a percutaneous needle aspiration, obtaining 50 mi of a purulent fluid. Due to persistence of fever, the patient was operated finding an inflammation that involved the mesentery and the great omentum and covering abscess. The pathologic study of the surgical piece reported a unspecific nodular mesenteric panniculitis.

Paniculitis mesentérica: infrecuente entidad clinicopatológica / Mesenteric panniculitis: a rare clinicopathological entity

Mesenteric panniculitis is an rare clinicopathological entity, presenting with a variety of manifestations, ranging from asymptomatic cases identified by image findings to retractile lesions that involve mesentery adjacent organs, such as bowel loops or encasement of the mesenteric vessels, producing ischemia and symptoms. A differential diagnosis should be established with other disorders, such as neoplasia, specially lymphoma when lymphnodesare present on the images. In general, it has a benign course, occasionally a biopsy sample is necessary to confirm the diagnosis. In symptomatic cases, improvement after use of steroids and immunomodulators has been observed. Surgery is an alternative treatment if a progressive course or a, lack of response to therapy are observed or when the diagnosis is uncertain.

La paniculitis mesentérica aparece como una entidad clinicopatológica infrecuente, con un abanico de manifestaciones, desde cuadros asintomáticos como hallazgos de estudio de imágenes, hasta lesiones retráctiles que comprometen órganos vecinos al mesenterio, como asas intestinales o engloban vasos mesentéricos produciendo isquemia y síntomas. Su presencia obliga a plantear el diagnóstico diferencial con otras entidades como los procesos neoplásicos entre ellos el linfoma, especialmente cuando se demuestran adenopatías en las imágenes. En general su evolución es benigna, en ocasiones es indispensable obtener biopsias para confirmar el diagnóstico. En casos sintomáticos el uso de corticoides e inmunomoduladores han sido de utilidad. La cirugía es una alternativa en casos de compromiso progresivo, falta de respuesta al tratamiento o duda diagnóstica.

Mesenteritis esclerosante: presentación de tres casos y revisión de la literatura / Sclerosing mesenteritis: presentation of three cases and review of the literature

Sclerosing mesenteritis or panniculitis is a rare condition characterized by inflammation of the mesentery ranging from an acute to a chronic fibrotic process that can resemble an intestinal malignant neoplasm even though it is benign. Its etiology is unknown, although it is thought to be the result of a nonspecific inflammatory response of the mesentery to an allergic, chemical, thermal, infectious, autoimmune or surgical stimulus. Its natural history is benign and in most cases is self-limited. Surgery is reserved only for those cases where there is intestinal obstruction. We report three cases of sclerosing mesenteritis that occurred after abdominal surgery and we present a review of the literature.

Mesenteric panniculitis. Imaging of a rare cause of chronic abdominal pain

We report a case of mesenteric panniculitis. This rare and poorly-known disease is characterized by a nonspecific inflammatory process involving the adipose tissue of the mesentery. This case illustrates its computerized tomographic and magnetic resonance imaging features and the value of imaging in differentiating it from other mesenteric diseases and thus, avoiding unnecessary surgery

Mesenteric panniculitis presenting as a huge retroperitoneal mass--a case report.

A rare case of mesenteric panniculitis occurring in a young patient and presenting as a huge retroperitoneal mass which was mistaken for malignancy, has been described.

Mesenteritis esclerosante: Una enfermedad de apariencia maligna / Sclerosing mesenteritis: a disease of malignant appearance

La mesenteritis esclerosante es una enfermedad rara, de etiología desconocida, y que a pesar de su frecuente apariencia neoplásica, es benigna. En el pasado se ha utilizado múltiples términos para referirse a esta entidad que tiene una presentación clínica variable y se caracteriza morfológicamente por un engrosamiento del mesenterio. Actualmente existe poca información acerca de su epidemiología, historia natural y respuesta al tratamiento. A continuación se presenta una revisión de la literautra y se discuten brevemente conceptos relevantes para el diagnóstico y tratamiento de paciente con mesenteritis esclerosante

Paniculite e mesentérica: revisão da literatura e apresentação de caso / Mesenteric panniculitis: literature review and case report

A paniculite mesentérica é uma entidade clínica rara. Aqui apresentamos um caso de um paciente de 71 anos, e, uma revisão da literatura foi feita analisando suas características clínicas (sinais e sintomas), suas complicações e seu prognóstico, bem como seu tratamento.

Mesenteric panniculitis, a very uncommon disease, was described by Jura in 1924, for the first time. The authors report a case of mesenteric panniculitis in a 71 years-old-man. The literature was widely reviewed and several controversies about clinical manifestations, etiology, macroscopic and microscopy findings are discussed. Finally the most adequate treatament for different complications of this desease were described.

Paniculitis mesenterica / Mesenteric panniculitis

Se reporta el caso de un paciente de 37 años, quien consultó por abdominal y otros síntomas inespecíficos, realizandose el diagnóstico de Paniculitis Mesentérica mediante el estudio histológico de un segmento de epiplón. Se revisan las caracteísticas clínicas de la Paniculitis Mesentérica y su diferencia con la Enfermedad de Weber-Christian