1.Clinical analysis of 11 cases of lymphoma complicated with paraneoplastic neurological syndrome.
Chong WEI ; Dan Qing ZHAO ; Yan ZHANG ; Wei WANG ; Wei ZHANG ; Dao Bin ZHOU
Chinese Journal of Hematology 2022;43(4):311-315
Objective: To evaluate the clinical characteristics, treatment, and prognosis of patients with paraneoplastic neurological syndrome (PNS) associated with lymphoma. Methods: Between January 2012 and May 2021, the clinical data of 11 patients with lymphoma complicated with PNS treated at Peking Union Medical College Hospital were retrospectively reviewed. Results: Among the 11 patients (8 male and 3 female) , the median onset age was 61 (range, 33-78) years. The symptoms of PNS preceded lymphoma in 10 patients. The median time from the onset of PNS to the diagnosis of lymphoma was 4 months. Of the 11 patients, one had Hodgkin's lymphoma, 8 had B-cell non-Hodgkin's lymphoma, and 2 had peripheral T-cell lymphoma. Seven patients were evaluated for onconeural antibody, of whom 2 were positive (1 for anti-Ma2 antibody and 1 for anti-Yo antibody) . Of the 11 patients, the PNS symptoms of 3 patients were located in the central nervous system, 4 were located in the peripheral nervous system, and 3 were located in the muscle. Eight of the 11 patients were treated with glucocorticoid-based immunosuppressive therapy before the diagnosis of lymphoma. Patients with central nervous system involvement and dermatomyositis responded well to glucocorticoid, whereas patients with peripheral neuropathy did not significantly benefit. All 11 patients were treated with chemotherapy after the diagnosis of lymphoma. The efficacy of chemotherapy was assessed in 9 patients, 7 cases achieved complete remission, 1 case was evaluated as stable disease, and 1 case was evaluated as disease progression. The PNS symptoms of the patients who achieved complete response were almost completely recovered. The median follow-up time was 42 (range, 4-95) months. At the end of the follow-up period, 6 of the 11 patients survived, 3 were lost to follow-up, and 2 died. The median overall survival of the whole group was not reached. Conclusions: PNS can involve various parts of the nervous system and can be associated with different types of lymphoma. Through early diagnosis and treatment, the PNS symptoms could improve in most patients who achieve complete remission of lymphoma.
Adult
;
Aged
;
Antibodies, Neoplasm
;
Autoantibodies
;
Female
;
Glucocorticoids
;
Humans
;
Lymphoma/diagnosis*
;
Male
;
Middle Aged
;
Paraneoplastic Syndromes, Nervous System/complications*
;
Retrospective Studies
2.Factors associated with long-term survival in critically ill patients following surgery for solid tumors complicated with paraneoplastic pemphigus.
Jia Xi PAN ; Sai Nan ZHU ; Shuang Ling LI ; Dong Xin WANG
Journal of Peking University(Health Sciences) 2022;54(5):981-990
OBJECTIVE:
Critically ill patients with solid tumors complicated with paraneoplastic pemphigus are usually treated in intensive care units (ICU) for perioperative management after surgical treatment. In this study, the clinical characteristics and predictors of long-term prognosis of these critically ill patients were analyzed.
METHODS:
the clinical and laboratory data of 63 patients with solid tumors complicated with paraneoplastic pemphigus admitted to ICU from 2005 to 2020 were retrospectively analyzed, and the survival status of the patients were followed up.
RESULTS:
Among the 63 patients, 79.4% had Castleman disease as the primary tumor, and 20.6% with other pathological types; 69.8% had severe-extensive skin lesions, and 30.2% had other skin lesions; the patients with bronchiolitis obliterans accounted for 44.4%, and 55.6% were not merged. Postoperative fungal infection occurred in 23.8% of the patients, and 76.2% without fungal infection. The median follow-up time was 95 months, and 25 patients died during the study period. The 1-year, 3-year and 5-year survival rates were 74.6% (95%CI 63.8%-85.4%), 67.4% (95%CI 55.6%-79.2%) and 55.1% (95%CI 47.9%-62.3%), respectively. The log-rank univariate analysis showed that the patients had age>40 years (P=0.042), preoperative weight loss>5 kg (P=0.002), preoperative albumin < 30 g/L (P < 0.001), paraneoplastic pemphigus complicated with bronchiolitis obliterans (P=0.002), and perioperative fungal infection (P < 0.001) had increased mortality. Cox univariate analysis showed that preoperative weight loss >5 kg (P=0.005), preoperative albumin < 30 g/L (P < 0.001), paraneoplastic pemphigus complicated with bronchiolitis obliterans (P=0.009), preoperative bacterial pulmonary infection (P=0.007), prolonged surgical time (P=0.048), postoperative oxygenation index (P=0.012) and low albumin (P=0.010) and hemoglobin concentration (P=0.035) in ICU, acute physiology and chronic health evaluation (APACHE Ⅱ) score (P=0.001); sequential organ failure assessment (SOFA) score (P=0.010), and postoperative fungal infection (P < 0.001) were risk factors for long-term survival. Cox regression model for multivariate analysis showed that preoperative weight loss > 5 kg (HR 4.44; 95%CI 1.47-13.38; P=0.008), and preoperative albumin < 30 g/L (HR 4.38; 95%CI 1.72-11.12; P=0.002), bronchiolitis obliterans (HR 2.69; 95%CI 1.12-6.50; P=0.027), and postoperative fungal infection (HR 4.85; 95%CI 2.01-11.72; P < 0.001) were independent risk factors for postoperative mortality.
CONCLUSION
The 5-year survival rate of critically ill patients undergoing surgery for paraneoplastic pemphigus combined with solid tumors is approximately 55.1%, with preoperative weight loss > 5 kg, albumin < 30 g/L, bronchiolitis obliterans and postoperative fungal infection were associated with an increased risk of near- and long-term postoperative mortality.
Adult
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Albumins/therapeutic use*
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Bronchiolitis Obliterans/pathology*
;
Critical Illness
;
Hemoglobins
;
Humans
;
Neoplasms/complications*
;
Paraneoplastic Syndromes/pathology*
;
Pemphigus/drug therapy*
;
Retrospective Studies
;
Weight Loss
4.A case of retroperitoneal Castleman's disease with paraneoplastic pemphigus.
Zhipeng ZHANG ; Maosong ZHOU ; Jin GUO ; Tiecheng FENG ; Xinying LI ; Huan CHEN ; Jindong LI
Journal of Central South University(Medical Sciences) 2016;41(5):548-552
Paraneoplastic pemphigus is a rare autoimmune bullous dermatosis, which is caused by potential neoplasm, especially the Castleman's disease. Castleman's disease associated with paraneoplastic pemphigus is misdiagnosed frequently and easily in clinical practices. Furthermore, it is reported that the mortality rate for this disease is very high. Bronchiolitis obliterans is the most common complication and the most important cause of death. There was a female patient presenting recalcitrant mucocutaneous erosions, ulcers and scattered erythemas in the body. The patient was diagnosed and treated for pemphigus vulgaris with little success in Xiangya Hospital, Central South University in January 2015. Further investigations confirmed the diagnosis of paraneoplastic pemphigus with retroperitoneal tumor. Subsequently, the patient was treated with tumor resection in combination with intravenous immunoglobulin and corticosteroids. The pathology revealed that it was the Castleman's disease. Her mucocutaneous performance recovered obviously and the bronchiolitis obliteran did not appear in the follow-up. Castleman's disease associated with paraneoplastic pemphigus should be considered when mucosal and skin lesions showing no improvement under corticosteroids. Early and complete removal of the tumor together with immunotherapy could be beneficial to the patient's prognosis.
Adrenal Cortex Hormones
;
therapeutic use
;
Castleman Disease
;
complications
;
therapy
;
Female
;
Humans
;
Immunoglobulins, Intravenous
;
therapeutic use
;
Paraneoplastic Syndromes
;
complications
;
therapy
;
Pemphigus
;
complications
;
therapy
;
Retroperitoneal Space
;
pathology
5.Cholangiocarcinoma with a paraneoplastic leukemoid reaction mimicking a pyogenic liver abscess.
Hyoju HAM ; Hee Yeon KIM ; Kyung Jin SEO ; Su Lim LEE ; Chang Wook KIM
The Korean Journal of Internal Medicine 2015;30(1):110-113
No abstract available.
Bile Duct Neoplasms/complications/*diagnosis
;
*Bile Ducts, Intrahepatic/chemistry/pathology/radiography
;
Biopsy
;
Cholangiocarcinoma/complications/*diagnosis
;
Diagnosis, Differential
;
Fever/diagnosis/*etiology
;
Humans
;
Immunohistochemistry
;
Leukocytosis/*diagnosis/etiology
;
*Liver/chemistry/pathology/radiography
;
Liver Abscess, Pyogenic/*diagnosis
;
Magnetic Resonance Imaging
;
Male
;
Middle Aged
;
Paraneoplastic Syndromes/*diagnosis/etiology
;
Predictive Value of Tests
;
Tomography, Spiral Computed
;
Tumor Markers, Biological/analysis
6.Heart failure as the first manifestation of renal cell carcinoma.
Chee Meng LEE ; Allen SIM ; Gunasegaran KURUGULASIGAMONEY ; Lay Guat NG
Korean Journal of Urology 2015;56(1):82-85
We report the rare case of a patient with advanced renal cell carcinoma (RCC) who initially presented to the hospital with symptoms of cardiac failure. Preoperative cardiac studies did not reveal any underlying ischemia. After resection of a large 14-cm left renal tumor, cardiac function was noted to improve dramatically. We discuss this case of concomitant RCC and nonischemic cardiomyopathy.
Asian Continental Ancestry Group
;
Carcinoma, Renal Cell/*diagnosis/surgery
;
Cardiomyopathies/*diagnosis
;
Female
;
Heart Failure/*etiology
;
Humans
;
Middle Aged
;
Paraneoplastic Syndromes/complications
;
Thalassemia/complications
7.Paraneoplastic Eosinophilia in Clear Cell Renal Cell Carcinoma.
Wei-Wei ZHOU ; You-Yan GUAN ; Xin-Min LIU
Chinese Medical Journal 2015;128(16):2271-2272
9.Dermatomyositis associated with hepatitis B virus-related hepatocellular carcinoma.
Suh Yoon YANG ; Bong Ki CHA ; Gihyeon KIM ; Hyun Woong LEE ; Jae Gyu KIM ; Sae Kyung CHANG ; Hyung Joon KIM
The Korean Journal of Internal Medicine 2014;29(2):231-235
Dermatomyositis is an idiopathic inflammatory myopathy with typical cutaneous manifestations. It has been proposed that dermatomyositis may be caused by autoimmune responses to viral infections. Previous studies have shown an association between dermatomyositis and malignant tumors such as ovarian cancer, lung cancer, and colorectal cancer. However, a chronic hepatitis B virus (HBV) infection associated with dermatomyositis and hepatocellular carcinoma (HCC) has been very rarely reported. Here, we report a rare case of dermatomyositis coinciding with HBV-associated HCC. A 55-year-old male was confirmed to have HCC and dermatomyositis based on proximal muscle weakness, typical skin manifestations, elevated muscle enzyme levels, and muscle biopsy findings. This case suggests that HCC and/or a chronic HBV infection may be factors in the pathogenesis of dermatomyositis through a paraneoplastic mechanism.
Antiviral Agents/therapeutic use
;
Biopsy
;
Carcinoma, Hepatocellular/diagnosis/*virology
;
Dermatomyositis/diagnosis/drug therapy/*virology
;
Disease Progression
;
Fatal Outcome
;
Glucocorticoids/therapeutic use
;
Hepatitis B, Chronic/*complications/diagnosis/drug therapy
;
Humans
;
Liver Neoplasms/diagnosis/*virology
;
Male
;
Middle Aged
;
Paraneoplastic Syndromes/diagnosis/drug therapy/*virology
;
Risk Factors
;
Time Factors
;
Tomography, X-Ray Computed
;
Treatment Outcome

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