Background: The purpose of this study was to evaluate the usefulness of strain elastography and acoustic radiation force impulse (ARFI) imaging in the differentiation of benign and malignant cervical lymph nodes (LNs). Materials and Methods: In this prospective study, 50 enlarged cervical LNs (33 benign and 17 malignant) were examined by B-mode ultrasound (US), color Doppler, and strain elastography. Elastographic patterns (1–5) were categorized based on distribution of hard area within LN. The shear wave velocity (SWV) of LNs was evaluated by ARFI imaging. Diagnostic performance of sonoelastographic parameters was compared taking histopathology of LN as a reference standard. Optimal cutoff value of the mean SWV values for predicting malignancy was determined using receiver operating characteristic curve analysis. Results: Among US parameters, borders of LN had the highest diagnostic accuracy (80%), while echogenicity had the least (48%). Majority of benign LNs ( n = 31) had elastography patterns 1 and 2, while majority of malignant LNs ( n = 16) had patterns 3–5 ( P = 0.000). The sensitivity, specificity, and accuracy of elastography were 94.1%, 93.9%, and 94%, respectively. The mean SWV of benign LNs (1.670 ± 0.367 m/s) differed significantly from malignant LNs (2.965 ± 0.826 m/s; P = 0.000). A cutoff value of 2.05 m/s predicted malignancy with 88.2% sensitivity and 84.8% specificity and gave an area under the curve of 0.949 (95% confidence interval: 0.70–1.20). Conclusion: Elastography has high diagnostic accuracy in differentiating benign and malignant cervical LNs and can be potentially useful in selecting the LN with high probability of malignancy, on which fine-needle aspiration cytology/biopsy can be performed.

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Background: Cushing’s syndrome (CS) in a patient with VHL has been attributed to a number of possible causes; pancreatic NET and renal cell carcinoma. The precise location of ectopic ACTH aid enormously in the management of VHL. Clinical case: A 31-year-old woman with Type 2 diabetes and family history of VHL presented with florid features of CS in her second trimester of pregnancy. A diagnosis of ACTH dependent CS was made based on elevated 24h urinary cortisol (1122 and 2448nmol/24hr, n<150-800), midnight cortisol (1322nmol/L, n<220nmol/L) and a detectable ACTH level (18.8pg/mL, n<10pg/mL). She underwent emergency caesarean section due to pre-eclampsia at 28 week gestation. Post-delivery, her morning cortisol was 2823nmol/L (n:171-536nmol/L). MRI pituitary was reported as normal. CT abdomen showed an enlarged pancreas which was almost completely cystic and a right renal mass (3.7 X 2.6 X 4cm). Serum chromogranin A was elevated (530.2ng/mL, n:27-94). 24h urinary free metanephrine was normal. Selective ACTH sampling was done together with bilateral inferior petrosal sinus sampling to elicit source of ACTH. Increased gradient of ACTH level compared to the periphery (138.9pg/mL vs. samples from IVC:115.1 pg/mL, renal vein:100.2 pg/mL) was detected from the hepatic vein that drains the pancreas via the portal venous system. Ketoconazole and metyrapone were given to control the cortisol level close to 600nmol/L prior to surgery. Preoperatively, IV hydrocortisone 100mg was administered, with additional 50mg given every 4 hours intraoperatively. Total pancreatectomy and right nephrectomy were performed. Inotropic support was required five hours into the surgery. Hydrocortisone was tapered down to a maintenance dose of 10mg, 5mg and 2.5mg TDS over 7 days. A week after surgery, am cortisol was 103nmol/L suggesting successful removal of ectopic ACTH source. Histopathological examination identified a solid tumour (18X12X12 mm) at the pancreatic tail which stained positive to Chromogranin A, synaptophysin and weakly positive to CD56. The mitoses was 0-1/10hpf with a Ki67 index of 2%. ACTH staining was positive. The renal mass was a Grade 1 clear cell renal cell carcinoma with equivocal ACTH staining. Two months later, there was resolution of cushingoid features. DOTATE and FDG/PET scans along with close surveillance using serum Chromogranin A and 6 monthly abdominal imaging were planned. Conclusion: When managing VHL with CS, there is always a possibility of more than one source of ACTH production. In delineating the cause of CS the use of selective ACTH sampling may be considered where functional imaging (DOTATATE) is unavailable. Reference : (1) Tamura K, Nishimori I, Ito T, Yamasaki I, Igarashi H, Shuin T. Diagnosis and management of pancreatic neuroendocrine tumor in von hippel-lindau disease. World J Gastroenterol . 2010;16(36):4515-4518. doi:10.3748/wjg.v16.i36.4515

Fetus in fetu is a rare condition associated with abnormal embryogenesis in a diamniotic, monochorionic pregnancy, wherein one of the fetus is enclosed within the body of another normally developing fetus. It should be differentiated from a teratoma because of the later’s malignant potential. Here we report a case of 2 months old girl child who presented with complaints of abdominal distension. USG showed a solid cystic retroperitoneal mass resembling an anencephalic fetus. Contrast enhanced Computed tomography (CT) showed similar findings with visualization of bones resembling femur, sacrum and vertebrae. Findings were correlated with MRI and post-op pathology. The preoperative diagnosis of FIF is based on the observation of vertebral column or limbs in a mass on imaging modalities and our case meets the required criteria.