1.Pain on finger tip treated by pricking blood of Jing-well points.
Chinese Acupuncture & Moxibustion 2011;31(5):440-440
Adult
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Bloodletting
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Female
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Fingers
;
pathology
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Humans
;
Middle Aged
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Pain Management
2.Acro-dermato-ungual-lacrimal-tooth syndrome: case report.
Jian YANG ; Hong-juan ZHANG ; Wen-lin YANG ; Guang-sheng CHEN ; Zhi-wei TANG ; Shuang CHEN ; Wen-hong YE
Chinese Medical Journal 2007;120(9):851-853
Adult
;
Ectodermal Dysplasia
;
genetics
;
pathology
;
Female
;
Fingers
;
abnormalities
;
Humans
;
Nasolacrimal Duct
;
abnormalities
;
Syndrome
;
Tooth Abnormalities
;
pathology
3.Bilateral Total Hip Arthroplasty in a Rare Case of Multicentric Reticulohistiocytosis.
Balaji SAIBABA ; Ramesh Kumar SEN ; Ashim DAS ; Aman SHARMA
Clinics in Orthopedic Surgery 2015;7(4):509-514
Multicentric reticulohistiocytosis (MRH) is a rare systemic disease, which commonly manifests as muco-cutaneous papulonodules and inflammatory erosive polyarthropathy. In this research, we report the clinical manifestations and management of a rare case of MRH with destructive arthropathy of bilateral hip joints and arthritis mutilans presenting with characteristic deformities. Disabling hip arthropathy that occurs secondary to MRH can be successfully managed with bilateral total hip arthroplasty (THA). Osteopenia and acetabular bone defects must be anticipated during THA. This case is reported due to its rare occurrence and because little literature has been published regarding THA in such patients.
*Arthroplasty, Replacement, Hip
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Fingers/pathology
;
Hip/pathology/radiography/surgery
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*Histiocytosis, Non-Langerhans-Cell
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Humans
;
Skin/pathology
;
Toes/pathology
4.Symmetric Lipofibromatous Hamartoma Affecting Digital Nerves.
Sung No JUNG ; Youngmin YIM ; Ho KWON
Yonsei Medical Journal 2005;46(1):169-172
Lipofibromatous hamartoma of the nerve is a benign tumor, which affects the major nerves and their branches in the human body. It is often found in the median nerve of the hand and is commonly associated with macrodactyly, but it is rarely found in the digital nerves at the peripheral level. This tumor is often found in young adults and may go through a self- limiting course. However, operation is indicated when the tumor size is large or when the associated nerve compressive symptoms are present. We have experienced a rare case of lipofibromatous hamartoma that symmetrically involved the volar digital nerves of both index fingers on the ulnar side. With the aid of a microscope, we dissected and removed the tumor as much as possible without sacrificing the nerve. No sensory change occurred in both fingers and no sign of recurrence was observed upon follow-up.
Adipose Tissue/pathology
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Adult
;
Female
;
Fingers/*innervation/pathology
;
Hamartoma/complications/*pathology
;
Humans
;
Nerve Compression Syndromes/etiology/*pathology
6.Hereditary Sclerosing Poikiloderma.
Hyo Jin LEE ; Dong Hoon SHIN ; Jong Soo CHOI ; Ki Hong KIM
Journal of Korean Medical Science 2012;27(2):225-227
Hereditary sclerosing poikiloderma (HSP) is a very rare disease. The clinical features are principally widespread poikiloderma and linear hyperkeratotic and sclerotic bands. We report an 18-yr-old male who presented reticular hyperpigmented lesions on the trunk and extremities since 2-yr-old. Also, linear sclerosing bands appeared on both antecubital and popliteal fossae after yr. Histopathologic finding showed dense sclerotic collagen fibers with telangiectasia in the upper dermis and fragmentations of damaged elastic fibers in the elastic stain, consistent with HSP. We report the first Korean case of HSP.
Abnormalities, Multiple
;
Adolescent
;
Elastic Tissue/pathology
;
Fingers/abnormalities
;
Humans
;
Hyperpigmentation/pathology
;
Male
;
Micrognathism/pathology
;
Rothmund-Thomson Syndrome/*diagnosis/pathology
;
Sclerosis/pathology
;
Skin Diseases/diagnosis/pathology
7.Macrodactylism Associated with Neurofibroma of the Median Nerve: A Case Report.
In Hee CHUNG ; Nam Hyun KIM ; Il Yong CHOI
Yonsei Medical Journal 1973;14(1):49-52
A case of macrodactyly associated with neurofiborma of the median nerve, a congenital anomaly of the hand, affecting only one(left middle) finger is reported with a review of the literature. Macrodactyly which is also termed local gigantism, megalodactylism, megalodactylia, or macrodactylism in other literature, is a rare congenital malformation characterized by overgrowth of one or more fingers of hand. Macrodactyly associated with neurofibroma of the median nerve is especially rare. For this reason the following case is presented together with a review of the literature.
Adolescent
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Angiography
;
Female
;
Fingers/abnormalities*
;
Fingers/radiography
;
Fingers/surgery
;
Human
;
Korea
;
Median Nerve*/surgery
;
Neurofibroma/complications*
;
Neurofibroma/pathology
;
Neurofibroma/surgery
;
Peripheral Nervous System Neoplasms/complications*
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Peripheral Nervous System Neoplasms/pathology
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Peripheral Nervous System Neoplasms/surgery
;
Radial Nerve/surgery
9.Current status of ultrasonography of the finger.
Seun Ah LEE ; Baek Hyun KIM ; Seon Jeong KIM ; Ji Na KIM ; Sun Young PARK ; Kyunghee CHOI
Ultrasonography 2016;35(2):110-123
The recent development of advanced high-resolution transducers has enabled the fast, easy, and dynamic ultrasonographic evaluation of small, superficial structures such as the finger. In order to best exploit these advances, it is important to understand the normal anatomy and the basic pathologies of the finger, as exemplified by the following conditions involving the dorsal, volar, and lateral sections of the finger: sagittal band injuries, mallet finger, and Boutonnière deformity (dorsal aspect); flexor tendon tears, trigger finger, and volar plate injuries (volar aspect); gamekeeper's thumb (Stener lesions) and other collateral ligament tears (lateral aspect); and other lesions. This review provides a basis for understanding the ultrasonography of the finger and will therefore be useful for radiologists.
Collateral Ligaments
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Congenital Abnormalities
;
Fingers*
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Pathology
;
Tears
;
Tendons
;
Thumb
;
Transducers
;
Ultrasonography*
;
Upper Extremity
;
Palmar Plate
10.Clinical diagnosis and treatment of giant cell tumor of tendon sheath in finger (70 cases report).
Xiao-Jun ZHANG ; Dong-Hong PEI ; Yong XI ; Hai-Xian WANG ; Yu WANG
China Journal of Orthopaedics and Traumatology 2012;25(12):1024-1026
OBJECTIVETo investigate surgical methods and therapeutic effects of giant cell tumor of tendon sheath in finger.
METHODSFrom July 2002 to December 2010,70 patients with giant cell tumor of tendon sheath in finger which confirmed by operation and pathology,were retrospectively analyzed. There were 29 males,41 females with an average of 42 years (ranged, 16 to 61), and the course of disease ranged form 4 months to 6 years (mean 11 months). The method of surgery and anesthesia were observed.
RESULTSAll wounds were got stage I healing,no necrosis occurred. Vascular crisis occurred in 6 cases (8.6%), inconformity of diagnosis in 18 cases (25.7%), changing of anesthesia due to situation of tumor in operation in 17 cases (24.3%). The patients were followed up from 2.2 to 10.5 years. Among them, 8 cases (11.4%) recurred, and diagnosied by the second operation without malignant change.
CONCLUSIONThe best anesthesia for giant cell tumor in finger should choose brachial plexus to fully expose,complete resection and less harmful damage; while the operation should complete resection at the stage I, and followed up actively, the second operation can be carried out for recorrenced.
Adolescent ; Adult ; Female ; Fingers ; surgery ; Giant Cell Tumors ; diagnosis ; pathology ; surgery ; Humans ; Male ; Middle Aged ; Tendons ; pathology ; surgery ; Young Adult