1.Clinical and pathological analysis of oral manifestations of 40 patients with secondary syphilis.
Hong HUA ; Zhi-min YAN ; Rui-tang SHI ; Yan GAO ; Yan-ying XU
Chinese Journal of Stomatology 2005;40(5):376-378
OBJECTIVETo analyze the clinical and pathological features of 40 patients with secondary syphilis.
METHODSA total of 40 cases of secondary syphilis confirmed by serology were collected during 1994-2004 and were first diagnosed on presentation with oral lesions.
RESULTSThe white patch in oral mucosa was found in 32 cases with painless or slight pain in most cases. The most common site of the lesion was the tongue. The histological examination on eight cases was initially misdiagnosed as oral candidosis or lichen planus, but confirmed as syphilis after serology revealed nonspecific inflammation with intraepithelial microabscess and dense perivascular infiltration of lymphocytes and plasma cells in connective tissue. The symptoms showed dramatic improvement in 16 cases after benzathine penicillin treatment.
CONCLUSIONSThe oral manifestations of syphilis have specific clinical and pathological feature and attention should be paid to the suspicious oral lesions when patients are first presented in a dental office.
Adult ; Female ; Humans ; Male ; Middle Aged ; Mouth Mucosa ; pathology ; Oral Ulcer ; etiology ; Syphilis ; complications ; diagnosis ; pathology
2.Analysis of Clinical Features and Risk Factors for Oral Ulcers and Bloodstream Infection in Patients with Hematopoietic Stem Cell Transplantation.
Ke WU ; Li-Na GUAN ; Jie-Yong ZHANG ; Ran ZHANG ; Zhi-Lei BIAN ; Chong WANG ; Ding-Ming WAN ; Wei-Jie CAO
Journal of Experimental Hematology 2023;31(3):866-870
OBJECTIVE:
To investigate the risk factors of oral ulcers and bloodstream infection in patients with hematopoietic stem cell transplantation.
METHODS:
The clinical data of 401 hematopoietic stem cell transplant patients in the First Affiliated Hospital of Zhengzhou University from January 2020 to December 2021 were retrospective analyzed, and the risk factors of oral ulcers and bloodstream infection statistical and analyzed.
RESULTS:
Among the 401 patients, the incidence of oral ulcers was 61.3% (246/401), and the incidence of bloodstream infection was 9.0% (36/401). A total of 40 strains of pathogenic bacteria were isolated from 36 patients, including 26 strains of Gram negative strains (65%), 13 strains of Gram positive strains (32.5%), and 1 strain of fungi (2.5%). Single-factor analysis showed that oral hygiene was associated with the occurrence of bloodstream infection, and the Multi-factor analysis showed that age ≥14 years old, disease diagnosis of leukemia, and allogeneic hematopoietic stem cell transplantation were risk factors for oral ulcers.
CONCLUSION
The incidence of oral ulcers in patients with hematopoietic stem cell transplantation is high. The age ≥14 years, disease diagnosis of leukemia, and allogeneic hematopoietic stem cell transplantation were risk factors for oral ulcers in patients, and oral hygiene was associated with the occurrence of bloodstream infection.
Humans
;
Adolescent
;
Retrospective Studies
;
Oral Ulcer/etiology*
;
Bacteremia/microbiology*
;
Hematopoietic Stem Cell Transplantation/adverse effects*
;
Sepsis
;
Risk Factors
;
Leukemia
3.Treatment of erosive oral lichen planus with topical tacrolimus.
Chinese Journal of Stomatology 2010;45(3):182-185
Administration, Topical
;
Humans
;
Immunosuppressive Agents
;
administration & dosage
;
adverse effects
;
therapeutic use
;
Lichen Planus, Oral
;
complications
;
drug therapy
;
pathology
;
Oral Ulcer
;
drug therapy
;
etiology
;
Tacrolimus
;
administration & dosage
;
adverse effects
;
therapeutic use
;
Treatment Outcome
4.Pyoderma gangrenosum with oral involvement - case report and review of the literature.
Geetha PARAMKUSAM ; Venkateswarlu MEDURI ; Naresh GANGESHETTY
International Journal of Oral Science 2010;2(2):111-116
Pyoderma gangrenosum (PG) is a rare, noninfectious neutrophilic dermatosis. Clinically, it begins with sterile pustules that rapidly progress into painful ulcers of variable depth and size with undermined violaceous borders. The diagnosis of PG is based on the history of an underlying disease, a typical clinical presentation, histopathology, and exclusion of other diseases. The peak incidence occurs between the ages of 20 to 50 years with women being more often affected than men. There have been very few reports of pyoderma gangrenosum with oral mucosal involvement. Oral lesions in previously reported cases have included ulcers of varying sizes from a few mm to several cm and have been reported to have been found on the tongue, soft and hard palate, buccal mucosa, and gingiva. Some of these oral lesions have been associated with ulcerative colitis, inflammatory bowel disease, and polycythemia rubra vera. A few cases were reported with biopsy findings, the histological picture being nonspecific, showing ulceration, and necrosis with inflammatory cell infiltrate. A peculiar case of pyoderma gangrenosum with an oral lesion is presented here, and the differential diagnosis is discussed.
Adult
;
Anti-Infective Agents
;
therapeutic use
;
Chlorhexidine
;
therapeutic use
;
Dapsone
;
therapeutic use
;
Drug Therapy, Combination
;
Female
;
Glucocorticoids
;
therapeutic use
;
Humans
;
Metronidazole
;
therapeutic use
;
Oral Ulcer
;
drug therapy
;
etiology
;
pathology
;
Prednisolone
;
therapeutic use
;
Pyoderma Gangrenosum
;
complications
;
Tooth Mobility
;
etiology
5.Complications of successively double autologous hemopoietic stem cell transplants.
Wen-Rong HUANG ; Wan-Ming DA ; Bo-Long ZHANG ; Chun-Ji GAO ; Xiao-Ping HAN ; Yu JING ; Xiao-Xiong WU ; Yu ZHAO ; Hong-Hua LI ; Quan-Shun WANG ; Yi-Zhuo ZHANG ; Jian BO
Journal of Experimental Hematology 2005;13(1):30-34
In order to get clinical information about safety and feasibility of successively double autologous hemopoietic stem cell transplants (SD-AHSCT) in malignant hematological disease patients, the complications and hematological reconstitution after SD-AHSCT in 20 patients were analyzed retrospectively. 20 patients with hematologic malignancies received autologous peripheral blood stem/progenitor cell transplantation at the first transplant, and then were given autologous bone marrow transplantation as the second transplant at 4-10 months. The results showed that all the patients tolerated mobilization and collection of peripheral blood stem/progenitor cells as well as bone marrow collection. All the patients got enough hematological stem/progenitor cells for SD-AHSCT and achieved hematological reconstitution after SD-AHSCT. The speed of hematological reconstitution was positively correlated with the transfused quantity of hematological stem/progenitor cells (r = 0.968). The hematological reconstitution after the first autologous hemopoietic stem cell transplant (AHSCT) was earlier than that of the second (P < 0.05). There was no statistical difference between the first and the second AHSCT for the incidence of skin or mucous membrane bleeding (P > 0.05). No patients occurred massive hemorrhage during SD-AHSCT. The quantity of platelet transfusion in the second AHSCT was larger than that in the first AHSCT (P < 0.01). The incidence of oral ulcer in the first AHSCT was significantly higher than that in the second (P < 0.01). No statistical difference between the first and the second AHSCT was there in infectious sites, infectious pathogens and infection incidence (P > 0.10). All the complications were improved or cured, and no patients died of SD-AHSCT complications. In conclusion, SD-AHSCT is safe and feasible, and worthy to be further popularized.
Adolescent
;
Adult
;
Female
;
Hematologic Neoplasms
;
surgery
;
Hematopoietic Stem Cell Transplantation
;
adverse effects
;
methods
;
Humans
;
Male
;
Oral Ulcer
;
etiology
;
Peripheral Blood Stem Cell Transplantation
;
adverse effects
;
methods
;
Platelet Transfusion
;
statistics & numerical data
;
Reproducibility of Results
;
Retrospective Studies
;
Transplantation, Autologous
6.Six years relapse-free treatment of a case with Langerhans cell histiocytosis grade III treated with thalidomide and prednisone.
Kang-you LI ; Yong-mei HU ; Jing-bo LÜ
Chinese Journal of Pediatrics 2012;50(11):865-866
Administration, Oral
;
Adolescent
;
Female
;
Histiocytosis, Langerhans-Cell
;
complications
;
drug therapy
;
pathology
;
Humans
;
Lymph Nodes
;
pathology
;
Prednisone
;
administration & dosage
;
therapeutic use
;
Retrospective Studies
;
Skin Ulcer
;
drug therapy
;
etiology
;
pathology
;
Thalidomide
;
administration & dosage
;
therapeutic use
;
Treatment Outcome
7.Molecular Analysis of Two Cases of Severe Congenital Neutropenia.
Joonhong PARK ; Myungshin KIM ; Jihyang LIM ; Yonggoo KIM ; Bin CHO ; Yeon Joon PARK ; Kyungja HAN
The Korean Journal of Laboratory Medicine 2010;30(2):111-116
Severe congenital neutropenia is a rare hematological disease characterized by a selective decrease in circulating neutrophils, maturation arrest of granulocytic precursors at the promyelocyte stage, and recurrence of infections. A 2-month-old male infant (patient A) and a 14-month-old female child (patient B) were referred to our hospital due to severe neutropenia. Sequencing analysis of ELA2 and HAX1 genes was performed. Two single nucleotide polymorphisms of HAX1 gene were found. They were 5,104T-->G point mutation of exon 1 and 5,474A-->G point mutation of intron 1 in HAX1 gene. The mutation of ELA2 gene was not found. The patient A showed a good response to granulocyte colony-stimulating factor (G-CSF) treatment and the absolute neutrophil count recovered to 1,195/microliter. But the patient B showed a partial response to G-CSF treatment and experienced several episodes of herpetic gingivostomatitis, oral ulcer, acute pharyngotonsillitis and otitis media during follow-up.
Adaptor Proteins, Signal Transducing/genetics
;
Bone Marrow/pathology
;
Female
;
Granulocyte Colony Stimulating Factor, Recombinant/adverse effects/therapeutic use
;
Humans
;
Infant
;
Male
;
Neutropenia/congenital/drug therapy/*genetics
;
Neutrophils/cytology/pathology
;
Oral Ulcer/etiology
;
Otitis Media/etiology
;
Polymorphism, Single Nucleotide
;
Serine Endopeptidases/genetics
;
Stomatitis, Herpetic/etiology