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Papillary Renal Cell Carcinoma Presenting with Hemoptysis Michael Dougan, PhD, HMSIII Gillian Lieberman, MD July 2009 Our patient • 57 y.o. man with a previous smoking history, and an 8 month history of COPD presenting with worsening dyspnea on exertion, cough, and wheezing • A chest X‐ray was performed to look for lung processes that could be acutely exacerbating his condition – – – – Pneumonia Obstruction/collapse Pneumothorax Pleural effusion Our patient’s initial evaluation by chest X-ray is shown below Frontal Upright Chest X-Ray BIDMC PACS Left Lateral Upright Chest X-Ray ABCs of CXR : quality control Frontal Upright Chest X-Ray Left Lateral Upright Chest X-Ray BIDMC PACS Is this our patient? Do we have the standard views? Is the entire region of interest covered? Exposure? ABCs of CXR : aberrant air Frontal Upright Chest X-Ray Left Lateral Upright Chest X-Ray BIDMC PACS ABCs of CXR : bones ABCs of CXR : cardiac silhouette Frontal Upright Chest X-Ray Left Lateral Upright Chest X-Ray BIDMC PACS ABCs of CXR : diaphragm ABCs of CXR : cardiac silhouette Frontal Upright Chest X-Ray Left Lateral Upright Chest X-Ray BIDMC PACS depressed diaphragm ABCs of CXR : cardiac silhouette Frontal Upright Chest X-Ray Left Lateral Upright Chest X-Ray BIDMC PACS small effusion ABCs of CXR : extras Frontal Upright Chest X-Ray BIDMC PACS outside the patient Left Lateral Upright Chest X-Ray ABCs of CXR : fields Frontal Upright Chest X-Ray BIDMC PACS Left Lateral Upright Chest X-Ray Increased markings ABCs of CXR : gastric bubble and hila Our patient’s course: worsening COPD • Our patient was released with a diagnosis of worsening COPD – no acute lung problem • 2 months later, he returned with a new COPD exacerbation, this time complicated by hemoptysis • Because of his acutely worsening condition, a CT scan was ordered Chest CT for to evaluate hemoptysis axial chest CT: lung window yellow oval: airspace filling DDx: water, blood, cells, protein BIDMC PACS orange oval: focal density could this be malignant? Right bronchial mass on CT coronal reconstruction CT of the chest: soft tissue window Yellow circle: density in the right bronchus malignancy? mucus plug? BIDMC PACS Incidental finding in the abdominal portion of the CT axial CT through the abdomen: soft tissue window pre-contrast yellow circle: exophytic posterior left kidney cyst post-contrast BIDMC PACS Overview of normal renal anatomy www.nlm.nih.gov/medlineplus/ency/imagepages/1101.htm Exophytic kidney cyst DDx Benign Cyst (common) Renal Tumor (RCC, TCC, other) Abscess Vascular Abnormality Metastasis Cystic Kidney Syndrome follow-up is determined by specific radiographic features www.nlm.nih.gov/medlineplus/ency/imagepages/1101.htm common incidental findings Bosniak Classification System • Bosniak I: hairline thin wall; no septa, calcification, or solid components. Water density, no enhancement. • Bosniak II: a few hairline thin septa, fine calcification in wall or septa. • Bosniak IIF: more hairline septa. Minimal septa or wall enhancement, minimal wall thickening. Nodular or thick calcifications. No soft tissue enhancement. • Bosniak III: cystic masses with thickened irregular walls, or septa with enhancement • Bosniak IV: Cystic lesions with enhancing soft-tissue elements Generally Benign Cysts (I, II) • Bosniak I: hairline thin wall; no septa, calcification, or solid components. Water density, no enhancement. • Bosniak II: a few hairline thin septa, fine calcification in wall or septa. • Bosniak IIF: more hairline septa. Minimal septa or wall enhancement, minimal wall thickening. Nodular or thick calcifications. No soft tissue enhancement. • Bosniak III: cystic masses with thickened irregular walls, or septa with enhancement • Bosniak IV: Cystic lesions with enhancing soft-tissue elements Potentially Malignant (IIF – IV) • Bosniak I: hairline thin wall; no septa, calcification, or solid components. Water density, no enhancement. • Bosniak II: a few hairline thin septa, fine calcification in wall or septa. • Bosniak IIF: more hairline septa. Minimal septa or wall enhancement, minimal wall thickening. Nodular or thick calcifications. No soft tissue enhancement. • Bosniak III: cystic masses with thickened irregular walls, or septa with enhancement • Bosniak IV: Cystic lesions with enhancing soft-tissue elements Follow-up Required Evidence that Bosniak criteria are clinically meaningful Bosniak Classification I % Malignant 1.8% (2/114) II 18.5% (20/108) III 33% (218/660) IV 92.5% (148/160) Analyzing our patient’s cyst using the Bosniak criteria axial CT through the abdomen: soft tissue window pre-contrast post-contrast yellow circles: exophytic cyst, soft tissue density, some regions of inhomogeneity, question of rim enhancement, calcified rim, accessory nodule. How should we classify our patient’s cyst? • Bosniak IIF: follow-up recommended – MRI can provide greater soft tissue detail Further diagnostic steps for our patient • Multiple pulmonary/bronchial nodules identified – Concern for primary pulmonary malignancy – Bronchial nodule was resected and sent to pathology • Follow-up MRI of the kidneys was performed to further characterize the mass Follow-up MRI was ordered BIDMC PACS Sagittal abdominal MRI: T1 pre-contrast fat suppressed yellow circle: posterior exophytic left kidney mass high signal regions suggest focal hemorrhage Sagittal abdominal MRI: T1 postcontrast fat suppressed orange circle: hyper-intensity in the posterior renal fat malignant invasion? inflammation? pink arrows: enhancing papillary nodules Coronal MRI of the kidney BIDMC PACS coronal abdominal MRI: T1 pre-contrast, fat suppressed coronal abdominal MRI: T1 post-contrast, fat suppressed pre-contrast images can be mathematically subtracted from post-contrast images to confirm regions of enhancement, outlining areas of blood flow Further analysis of blood flow by MRI coronal abdominal MRI: post-contrast subtraction view BIDMC PACS pink arrows: enhancing papillary nodules MRI aided diagnosis • MRI imaging findings are characteristic of papillary RCC – – – – Cystic mass Well encapsulated Relatively low/homogenous enhancement with gadolinium Enhancing, papillary projections into lumen • Diagnosis was confirmed by bronchoscopy – The mass in his bronchus was confirmed to be papillary RCC Renal cell carcinoma • Most common tumor of the kidney Clear Cell RCC • Subtypes of RCC – – – – – Clear Cell (75% – 85%) Chromophilic/papillary (10% – 15%) Chromophobic (5% – 10%) Oncocytic (rare) Collecting Duct (rare) http://pathologyoutlines.com Papillary RCC http://pathologyoutlines.com RCC staging and prognosis • Staging – – – – Stage I: < 7 cm Stage II: > 7 cm but limited to kidney Stage III: invasion into veins, adrenal, perirenal space Stage IV: invasion beyond perirenal fascia, including distant metastases Stage Prognosis (5 year survival) I 91% ‐ 100% II 74% ‐ 96% III 59% ‐ 70% IV 16% ‐ 32% Use of CT for staging RCC • Detect invasion of perirenal structures (Stage III disease) – Veins (renal, IVC) – Adrenal Gland – Perirenal fasica • Identify distant metastases (Stage IV disease) – e.g. the pulmonary masses in our patient? • Other modalities include: – MRI, metabolic bone scan, PET • Clear cell RCC is more common than the papillary variant, and has a more typical, malignant presentation by CT using the Bosniak criteria as demonstrated by companion patient 1 Companion patient 1: typical presentation of clear cell RCC BIDMC PACS Post contrast axial CT through the abdomen: soft tissue window Yellow circle: complex cystic mass (Bosniak IV) Orange rectangle: area of detail (next slide) Magnification view Post contrast axial CT through the abdomen centered on IVC: soft tissue window BIDMC PACS complex cystic mass (Bosniak IV) Yellow oval: tumor thrombus in the IVC (stage III disease) Renal cell carcinoma treatment • Surgical Resection (Stage I – III only) • Standard chemotherapy has not been found to be effective • Immune Therapy – IL-2, Interferon alpha, bevacizumab • Targeted Therapy (Stage III, IV) – mTOR (temsirolimus), VEGF Receptor (sunitinib, sorafenib) • Clinical Trials – response rates to current therapeutic regimens are poor Immune therapy for RCC • Tumors often express proteins that can be recognized as foreign by the immune system – Mutated proteins, developmental/tissue restricted proteins, etc. • Spontaneous anti-tumor immune responses do occur, but are rare and often insufficient to clear tumors • Immune therapy is used to augment nascent anti-tumor immune responses – cytokines, monoclonal antibodies Cytokine therapy mechanism of action • Both IL-2 and interferon alpha are important factors in promoting immune responses • IL-2: potent T cell growth factor • Interferon alpha: critical in for anti-viral responses, makes infected cells (or tumors) more susceptible killing by cytotoxic cells (CD8 T cells, and NK cells) Cytokine therapy efficacy and side effects • Objective response rates are currently low (~10%), and durable responses are rare • Adverse effects are significant, and resemble those of influenza infection – Malaise, fever, night sweats, joint pain, nausea Monoclonal antibody therapy for RCC • Vascular Endothelial Growth Factor (VEGF) is an important growth factor in RCC – important in renal tumors associated with VHL disease • VEGF can be directly targeted by monoclonal antibody therapy (bevacizumab) – Also targeted by new small molecule inhibitors (currently the treatment of choice for many patients due to improved tolerability) Follow up on our patient • Diagnosed with Stage IV papillary RCC with intrabronchial metastases • Poor prognosis, limited response to current therapies • Entered into a clinical trial investigating a novel small molecule inhibitor Conclusion • Incidental renal cysts are a common finding • Renal cysts are classified radiographically using the Bosniak system to separate benign findings from probable malignancies • MRI can play an important role in correctly diagnosing cysts with indeterminate features on CT • RCC is the most common tumor of the kidney, and, in early stage disease (stage I and II), can be treated by surgery alone • Advanced RCC has a poor prognosis, and is managed using immune therapy or using targeted molecular therapy Acknowledgments • Erica Gupta • Maryellen Sun • Gillian Lieberman • • • • • • • Glenn Dranoff Richard Haspel Adam Jeffers Jay Pahade Rich Rana Aarti Sekhar Jennifer Son References • • • • • • • • Balci NC, Semelka RC, Patt RH, Dubois D, Freeman JA, Gomez‐Caminero A, Woosley JT. 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