1.Pulmonary alveolar microlithiasis: report of a case.
Hong-sheng LU ; Tao ZHOU ; Mei-fu GAN
Chinese Journal of Pathology 2007;36(5):348-349
Adult
;
Biopsy
;
Follow-Up Studies
;
Humans
;
Lithiasis
;
diagnostic imaging
;
pathology
;
surgery
;
Lung
;
diagnostic imaging
;
pathology
;
surgery
;
Lung Diseases
;
diagnostic imaging
;
pathology
;
surgery
;
Male
;
Pulmonary Alveoli
;
diagnostic imaging
;
pathology
;
surgery
;
Tomography, X-Ray Computed
2.Cardiac papillary fibroelastoma: report of a case.
Hong-Sheng LU ; Mei-Fu GAN ; Wen-Sheng HAN ; Han-Song CHEN
Chinese Journal of Pathology 2008;37(5):358-360
Adult
;
Female
;
Fibroma
;
etiology
;
Heart Neoplasms
;
pathology
;
physiopathology
;
Humans
;
Leiomyoma
;
physiopathology
3.Microscopic thymoma: report of two cases.
Hong-sheng LU ; Mei-fu GAN ; Gang SUN ; Wei-fei CHEN
Chinese Journal of Pathology 2010;39(2):124-125
Adult
;
Antibodies, Monoclonal
;
analysis
;
DNA Nucleotidylexotransferase
;
metabolism
;
Female
;
Follow-Up Studies
;
Humans
;
Keratins
;
immunology
;
Male
;
Middle Aged
;
Prognosis
;
Thymoma
;
metabolism
;
pathology
;
surgery
;
Thymus Neoplasms
;
metabolism
;
pathology
;
surgery
4.Uterine epithelioid trophoblast tumor: report of a case.
Mei-fu GAN ; Chun-kai YU ; Hong-sheng LU ; Pei-nong YANG
Chinese Journal of Pathology 2007;36(8):570-571
Abdominal Neoplasms
;
secondary
;
surgery
;
Abdominal Wall
;
Antiporters
;
metabolism
;
Choriocarcinoma
;
pathology
;
Diagnosis, Differential
;
Epithelioid Cells
;
pathology
;
Female
;
Gestational Trophoblastic Disease
;
metabolism
;
pathology
;
secondary
;
surgery
;
Humans
;
Pregnancy
;
Uterine Neoplasms
;
metabolism
;
pathology
;
surgery
;
Young Adult
5.Primary myxoid liposarcoma of the pericardium.
Mei-fu GAN ; Hong-sheng LU ; Shou-xiang WENG ; Ju-fang CAI ; Wei-guang BAO
Chinese Journal of Pathology 2006;35(3):185-186
Adult
;
Diagnosis, Differential
;
Heart Neoplasms
;
metabolism
;
pathology
;
surgery
;
Humans
;
Immunohistochemistry
;
Liposarcoma, Myxoid
;
metabolism
;
pathology
;
surgery
;
Male
;
Myxoma
;
metabolism
;
pathology
;
Myxosarcoma
;
metabolism
;
pathology
;
Pericardium
;
S100 Proteins
;
metabolism
;
Vimentin
;
metabolism
6.Treatment of atrophic rhinitis by transplantation of pediculated bone-suberiosteal muscle flap
Yong-Gan WANG ; Qian-Mei SHI ; Yan-Hong WANG ; Chun-Jiu HU ; Zhong-Ming LIN ; Tao GUO ; Rong-Sheng NI ;
Chinese Journal of Primary Medicine and Pharmacy 2006;0(10):-
Objective To explore a better method for treatment atrophic rhinitis.Methods 56 patients with atrophic rhinitis(96 lateral)were treated by nasal submucou pediculated bone-suberiosteal muscle flap extracted from anterior wall of sinus maxillaries.Results All patients were followed 2 to 10 years,total effective rate was 100 %, with 49 cases(87.5 %)showing prominent effect.Conclusion The grafted flap cannot be assimilated,felled off and necrosis,because the flap has rich blood supply.This methods has obvious short-term effective and stable long-term effective.No complications were found.
8.Adrenal myelolipoma within myxoid cortical adenoma associated with Conn's syndrome.
Hong-sheng LU ; Mei-fu GAN ; Han-song CHEN ; Shan-qiang HUANG
Journal of Zhejiang University. Science. B 2008;9(6):500-505
The coexistence of myelolipoma within adrenal cortical adenoma is extremely rare, for both tumors present usually as separate entities. There are only 16 such cases reported worldwide. To the best of our knowledge, the case we reported here is the first one of myxoid adrenal cortical adenoma associated with myelolipoma reported. A 32-year-old Chinese woman with 4-year history of hypertension was presented in our study. Computed tomography (CT) of the abdomen showed a large heterogeneously-enhancing mass (4.5 cm in diameter) in the left suprarenal region. Clinical history and laboratory results suggest a metabolic disorder as Conn's syndrome. The patient underwent a left adrenalectomy, and a histopathological study confirmed the mass to be a myxoid adrenal cortical adenoma containing myelolipoma. The patient was postoperatively well and discharged uneventfully. In the present case report, we also discuss the etiology of simultaneous myelolipoma and adrenal adenoma associated with Conn's syndrome, and the methods of the diagnosis and differential diagnosis.
Adrenal Cortex Neoplasms
;
complications
;
diagnosis
;
pathology
;
Adrenocortical Adenoma
;
complications
;
diagnosis
;
pathology
;
Adult
;
Biomarkers, Tumor
;
metabolism
;
Female
;
Humans
;
Hyperaldosteronism
;
complications
;
Inhibins
;
metabolism
;
Myelolipoma
;
complications
;
diagnosis
;
pathology
;
Neoplasms, Multiple Primary
;
complications
;
diagnosis
;
pathology
;
Synaptophysin
;
metabolism
;
Tomography, X-Ray Computed
;
Vimentin
;
metabolism
9.Interdigitating dendritic cell sarcoma/tumor: a study of 3 cases.
Mei-Fu GAN ; Hong-Sheng LU ; Jian-Wei ZHANG ; Xin-Ru YU
Chinese Journal of Pathology 2008;37(10):676-679
OBJECTIVETo study the pathologic features, diagnosis and differential diagnosis of interdigitating dendritic cell sarcoma (IDCS).
METHODSThe clinical findings, morphologic features and immunophenotype of 3 cases of IDCS were investigated.
RESULTSGross examination showed that IDCS had a greyish-white to greyish-yellow cut surface. The site of occurrence included lung, spleen (with lymph node metastasis) and lymph node. Histologically, the tumor cells were arranged in nests, fascicles and whorls, with intimate admixture of many lymphocytes and plasma cells. They were oval to spindle in shape and contained pale eosinophilic cytoplasm, oval and sometimes grooved nuclei, small distinct nucleoli and ill-defined cell borders. Immunohistochemical study showed that the tumor cells expressed S-100 protein.
CONCLUSIONSIDCS is a rare type of histiocytic and dendritic cell malignancy with distinctive morphologic findings. It needs to be distinguished from follicular dendritic cell sarcoma, inflammatory pseudotumor, Langerhans' cell histiocytosis, malignant melanoma, undifferentiated carcinoma and anaplastic large cell lymphoma. Immunohistochemical staining for S-100 protein is helpful in confirming the diagnosis.
Adolescent ; Carcinoma ; pathology ; Dendritic Cell Sarcoma, Follicular ; pathology ; Dendritic Cell Sarcoma, Interdigitating ; diagnosis ; pathology ; Dendritic Cells ; pathology ; Diagnosis, Differential ; Female ; Humans ; Lymph Nodes ; pathology ; Lymphatic Metastasis ; pathology ; Male ; Middle Aged ; S100 Proteins ; analysis ; immunology ; Young Adult
10.Extranodal Rosai-Dorfman disease.
Mei-fu GAN ; Tao ZHOU ; Xin-ru YU ; Chun-kai YU ; Hai-hong ZHENG ; Ju-fang CAI
Chinese Journal of Pathology 2005;34(3):137-139
OBJECTIVETo investigate the diagnosis and differential diagnosis of extranodal Rosai-Dorfman disease.
METHODSTwo cases of extranodal Rosai-Dorfman disease were studied using hematoxylin-eosin, and immunohistochemical staining, along with a literature review.
RESULTSThe lesions of RDD were characterized by the presence of large histiocytes with emperipolesis, accompanied by infiltration of lymphocytes, plasma cells and other inflammatory cells. The large histiocytes had an abundant cytoplasm, pale to eosinophilic in appearance, positive for S-100 protein staining, with a vesicular nucleus and a small basophilic nucleolus in each cell.
CONCLUSIONSExtranodal Rosai-Dorfman disease is known as an idiopathic proliferative disease of histiocytes with a distinct morphologic feature and is very rare. Differential diagnosis from other types of fibrohistiocytic proliferation lesions is recommended.
Antigens, CD ; metabolism ; Antigens, Differentiation, Myelomonocytic ; metabolism ; Brain ; pathology ; surgery ; Brain Diseases ; metabolism ; pathology ; surgery ; Dermatologic Surgical Procedures ; Diagnosis, Differential ; Histiocytosis, Sinus ; metabolism ; pathology ; surgery ; Humans ; Male ; Middle Aged ; S100 Proteins ; metabolism ; Skin ; pathology ; Skin Diseases ; metabolism ; pathology ; surgery