Cavernous hemangioma of colon and pregnancy: A case report

Cavernous hemangioma of the colon is a rare vascular malformation but is clinically important because it can sometimes cause massive bleeding. We report a case of thrombocytopenia in a post-partum young woman with large cavernous hemangioma of the ileum and colon, culminating in Kasabach Merritt syndrome (KMS), massive uncontrollable hemorrhage, and death. CT scan shows multiple submucosal bulgings in all segments of the colon. Macroscopic examination showed multiple well-defined masses, with gray-brown color in ileum, cecum and ascending colon. The masses were found to be a cavernous hemangioma with a thick fibrotic wall and extensive intra-cystic hemorrhage. KMS is an uncommon complication of colonic large hemangiomas that, as in our patient, can lead to uncontrollable bleeding and death and should be kept in mind by visceral surgeons as one differential diagnosis of large intra-abdominal tumorous masses, especially in young adults. © 2018 Tehran University of Medical Sciences. All rights reserved

Cavernous hemangioma of colon and pregnancy: A case report

Cavernous hemangioma of the colon is a rare vascular malformation but is clinically important because it can sometimes cause massive bleeding. We report a case of thrombocytopenia in a post-partum young woman with large cavernous hemangioma of the ileum and colon, culminating in Kasabach Merritt syndrome (KMS), massive uncontrollable hemorrhage, and death. CT scan shows multiple submucosal bulgings in all segments of the colon. Macroscopic examination showed multiple well-defined masses, with gray-brown color in ileum, cecum and ascending colon. The masses were found to be a cavernous hemangioma with a thick fibrotic wall and extensive intra-cystic hemorrhage. KMS is an uncommon complication of colonic large hemangiomas that, as in our patient, can lead to uncontrollable bleeding and death and should be kept in mind by visceral surgeons as one differential diagnosis of large intra-abdominal tumorous masses, especially in young adults. © 2018 Tehran University of Medical Sciences. All rights reserved

A Sporadic Desmoid Tumor: an Exceptional Pancreatic Cystic-Solid Mass

Desmoid tumors are locally aggressive and non-metastatic neoplasms with a high rate of recurrence. Desmoid tumors of the pancreas are, however, very rare, and only a few cases have been reported in the literature. This paper reports an anecdotal case of a diffuse pancreatic desmoid tumor with the involvement of the pancreatic head, body, and�partially�tail. The patient underwent the Whipple procedure and subtotal pancreatectomy. Histopathological assessment showed that the tissues were partly positive for smooth muscle actin, but not for S100 or PanCK. The Ki67 index of the cells was only 1 . Unfortunately, the patient died on the 10th postoperative day due to massive upper gastrointestinal bleeding. © 2015, Association of Surgeons of India

Usefulness of prolactin measurement in inferior petrosal sinus sampling with desmopressin for Cushing�s syndrome

Background: Bilateral inferior petrosal sinus sampling (IPSS) is used to distinguish pituitary from ectopic adrenocorticotropin (ACTH) excess in patients with ACTH-dependent Cushing�s syndrome. Our objective was to examine the utility of prolactin measurement during IPSS with desmopressin (DDAVP) stimulation in localization of the source of ACTH excess. Method: Retrospective review of 20 patients with ACTH-dependent Cushing�s syndrome who underwent IPSS with DDAVP stimulation. Baseline, DDAVP-stimulated, and prolactin-normalized ACTH IPS:P (inferior petrosal sinus to peripheral) ratios were calculated. Cut-off values for each test were obtained from receiver-operating characteristic (ROC) curve analysis. Results: Fifteen patients had Cushing disease (CD), and five were diagnosed with ectopic ACTH syndrome (EAS). For the baseline ACTH IPS:P ratio of �2, the diagnostic sensitivity (80), specificity (100), positive predictive value (PPV) (100) and negative predictive value (NPV) (62.5) were calculated. These values for DDAVP-stimulated IPS:P ACTH ratio � 3, were 86.7, 100, 100 and 71.4, respectively. The corresponding value for the prolactin-normalized ACTH IPS:P ratio � 0.8 were 86.6, 80, 92.8 and 66.7. The cut-off value for the baseline, DDAVP-stimulated and prolactin-normalized ACTH IPS:P ratios were 1.76, 3.9, and 0.33, respectively. Conclusion: Prolactin-normalized ACTH IPS:P ratio measurement showed comparable sensitivity and less specificity than baseline/DDAVP-stimulated IPS/P ACTH ratios. Moreover, when baseline and stimulated IPS/P ACTH tests were discordant, prolactin-normalized ACTH IPS: P ratio correctly localized the source of ACTH excess. The sensitivity of the test increased, applying a prolactin-normalized ACTH IPS: P ratio �0.33. © 2020, © 2020 The Neurosurgical Foundation

Usefulness of prolactin measurement in inferior petrosal sinus sampling with desmopressin for Cushing�s syndrome

Background: Bilateral inferior petrosal sinus sampling (IPSS) is used to distinguish pituitary from ectopic adrenocorticotropin (ACTH) excess in patients with ACTH-dependent Cushing�s syndrome. Our objective was to examine the utility of prolactin measurement during IPSS with desmopressin (DDAVP) stimulation in localization of the source of ACTH excess. Method: Retrospective review of 20 patients with ACTH-dependent Cushing�s syndrome who underwent IPSS with DDAVP stimulation. Baseline, DDAVP-stimulated, and prolactin-normalized ACTH IPS:P (inferior petrosal sinus to peripheral) ratios were calculated. Cut-off values for each test were obtained from receiver-operating characteristic (ROC) curve analysis. Results: Fifteen patients had Cushing disease (CD), and five were diagnosed with ectopic ACTH syndrome (EAS). For the baseline ACTH IPS:P ratio of �2, the diagnostic sensitivity (80), specificity (100), positive predictive value (PPV) (100) and negative predictive value (NPV) (62.5) were calculated. These values for DDAVP-stimulated IPS:P ACTH ratio � 3, were 86.7, 100, 100 and 71.4, respectively. The corresponding value for the prolactin-normalized ACTH IPS:P ratio � 0.8 were 86.6, 80, 92.8 and 66.7. The cut-off value for the baseline, DDAVP-stimulated and prolactin-normalized ACTH IPS:P ratios were 1.76, 3.9, and 0.33, respectively. Conclusion: Prolactin-normalized ACTH IPS:P ratio measurement showed comparable sensitivity and less specificity than baseline/DDAVP-stimulated IPS/P ACTH ratios. Moreover, when baseline and stimulated IPS/P ACTH tests were discordant, prolactin-normalized ACTH IPS: P ratio correctly localized the source of ACTH excess. The sensitivity of the test increased, applying a prolactin-normalized ACTH IPS: P ratio �0.33. © 2020, © 2020 The Neurosurgical Foundation

Cell proliferation, apoptosis, and angiogenesis in non-functional pituitary adenoma: association with tumor invasiveness

Purpose: Non-functioning pituitary adenoma (NFPA) is the most prevalent pituitary macroadenoma. No prognostic marker has been found to explain the behavior of these tumors. We aimed to explore cell proliferation, apoptosis, proangiogenic markers, and microvascular density (MVD) in noninvasive and invasive NFPAs. Methods: Adenoma invasiveness was defined according to Knosp and Hardy classifications based on preoperative magnetic resonance imaging scans. Cell proliferation was examined using Ki67 and P53. Tissue expression of Bcl-2 was used to assess the antiapoptosis pathway. CD34 and CD105 were measured to evaluate MVD, while VEGF expression was assessed as an indicator of pro-angiogenesis. Moreover, VEGF, bFGF, endocan, and endostatin were measured on preoperative serum samples. Results: Tissue and serum markers were examined in 18 patients with invasive and 21 patients with noninvasive NFPAs. Ki67 less than 3 was reported in 10 invasive and 14 noninvasive NFPAs (P = 0.752). P53 staining was negative in all subjects. In addition, Bcl-2 staining was negative in 15 and 20 subjects, respectively (P = 0.718). VEGF-A expression 2+ or 3+ was reported in 9 invasive and 11 noninvasive macroadenomas (P = 0.83). Moreover, CD34 and CD105 positivity were comparable between the two groups. Furthermore, the comparison of serum markers showed no significant differences. Conclusion: Cell proliferation, apoptosis, and angiogenesis play a limited role in NFPA behavior. © 2020, Springer Science+Business Media, LLC, part of Springer Nature

Primary bone marrow lymphoma: an uncommon extranodal presentation of aggressive non-hodgkin lymphomas.

Item does not contain fulltextBone marrow involvement by lymphoma is considered a systemic dissemination of the disease arising elsewhere, although some tumors may arise primarily in the bone marrow microenvironment. Primary bone marrow lymphoma (PBML) is a rare entity whose real boundaries and clinicobiological significance are not well defined. Criteria to diagnose PBML encompass isolated bone marrow infiltration, with no evidence of nodal or extranodal involvement, including the bone, and the exclusion of leukemia/lymphomas that are considered to primarily involve the bone marrow. Twenty-one out of 40 lymphomas retrospectively reviewed by the International Extranodal Lymphoma Study Group from 12 institutions in 7 different countries over a 25-year period fulfilled the inclusion criteria. These cases comprised 4 follicular lymphomas (FLs), 15 diffuse large B-cell lymphomas (DLBCLs), and 2 peripheral T-cell lymphomas, not otherwise specified. The FL cases showed paratrabecular infiltration, BCL2 protein and CD10 expression, and BCL2 gene rearrangement. DLBCL showed nodular infiltration in 6 cases and was diffuse in 9 cases; it also showed positivity for BCL2 protein (9/10) and IRF4 (6/8). Median age was 65 years with male predominance. All but 3 FL patients were symptomatic. Most cases presented with cytopenias and high lactate dehydrogenase. Four patients (3 FL cases and 1 DLBCL case) had leukemic involvement. Most DLBCL patients received CHOP-like or R-CHOP-like regimens. The outcome was unfavorable, with a median overall survival of 1.8 years. In conclusion, PBML is a very uncommon lymphoma with particular clinical features and heterogenous histology. Its recognition is important to establish accurate diagnosis and adequate therapy.1 februari 201