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By V. Navaras. University of Tennessee, Martin.
A 5-year-old girl is brought to the office by her mother after a fall that caused a forehead laceration order 250mg keflex visa antibiotics effect on liver. The fall was unwitnessed and occurred during the care of a babysitter cheap keflex 750 mg online antibiotic resistance quiz. The child has been in good health, though she has been slower than other children her age in reaching the usual milestones in cognitive development. On examination, the patient is a fair-skinned, dark-haired child with a streak of gray hair on the left scalp. She has a 2 cm laceration on her forehead, with considerable associated swelling. A Wood lamp examination reveals four pale, elongated mac- ules on her trunk. Which disorder best accounts for the findings in this case? Tuberous sclerosis Key Concept/Objective: To be able to recognize tuberous sclerosis by a finding of hypopigmented macules in the setting of likely mental retardation, seizures, and facial angiofibromas Tuberous sclerosis presents in infants and young children with a classic triad of hypopig- mented, ash-leaf-shaped macules (including those in the scalp, which cause gray streaks of hair), mental retardation, and seizures, though the last two can be absent. This child’s unwitnessed fall could have been a seizure, and her slowness to attain developmental mile- stones may be a sign of mental retardation. The finding of facial neurofibromas, skin-col- ored-to-red papules, is pathognomonic. In contrast, skin findings in neurofibromatosis include hyperpigmented, not hypopigmented, macules, as well as nodular neurofibromas in distributions other than the face. Pityriasis alba affects young children, usually those with dark skin. The lesions are usually on the face and may begin with subtle erythema and slightly raised borders. The lesions then become scaly, hypopigmented macules with indistinct borders and regress spontaneously after several months. Vitiligo causes depig- mentation of skin and hair that develops in older children and young adults, usually those of darker skin color. Associated conditions include autoimmune endocrine disorders but not seizures or retardation. Piebaldism causes a white forelock in 90% of patients, as well as amelanotic macules on the trunk, extremities, and mucous membranes. These are pres- ent at birth and remain stable over time, unlike vitiligo, which develops later in life and is often progressive. A 24-year-old Hispanic woman has been using oral contraceptives and was treated with ciprofloxacin for a bladder infection several months ago. She presents with concerns about some spots on her face that she would like to have removed. The spots appeared suddenly over the past few weeks. On examination, the patient has blotchy, hyperpigmented, brown macules over the central face, without scaling or induration, involving the nose, nasolabial folds, upper lip, cheeks, and forehead. There are no lesions on the oral mucosa and no rashes elsewhere on her body. What is the most likely cause of this patient’s hyperpigmented lesions? Drug-induced sun sensitivity Key Concept/Objective: To recognize melasma in patients with risk factors and characteristic skin findings Melasma causes hyperpigmented macules in the central areas of the face. Risk factors for melasma include dark skin, female gender, oral contraceptive use, pregnancy, and sun exposure. Tinea faciei can cause hyperpigmented lesions on the face, but these are usually scaly, with annular accentuation of hyperpigmentation and central clearing. Lichen planus is usually quite itchy and usually occurs in locations such as the wrists, back, shins, and buccal mucosa, but it can also involve the eyelids, tongue, lips, or scalp. Lichen planus is usually more violaceous in color and contains fine, parallel, lacy white lines called Wickham striae. Lupus can cause a malar rash, which is usually erythematous rather than brown and usually confluent rather than blotchy, with some associated fine scaling. Like melasma, this classic malar rash can worsen with sun exposure, but it spares the nasolabi- al folds. Drug-induced sun sensitivity should also spare the nasolabial folds and upper lip because these areas receive less sun exposure than do other areas of the face.
Neutral injured knee and she was anxious to have the alignment buy cheap keflex 750 mg on line antibiotic resistance uptodate, pronated feet discount keflex 500mg otc antibiotic upset stomach, squinting patellae, same surgery on the noninjured limb. Failure of Patellofemoral Surgery: Analysis of Clinical Cases 345 Figure 21. Pre-op CT rotational scan shows bilateral 54° femoral anteversion. A 37-year-old woman with 6 months of 12° R and 14° L, cruciate and collateral liga- constant pain in both knees requiring narcotic ments intact, significant pain with palpation medication. Anterior knee pain began 19 along the medial joint line on the right, prone years earlier. Two years later, 17 years ago, she internal hip rotation 50°, external rotation underwent a medial transfer of the left tibial 25°. Fifteen years ago she underwent a located excessively medial and the feet were medial transfer of the right tibial tubercle. Twelve years ago she underwent flexion weight bearing showed equal joint arthroscopy with lysis of adhesions followed space medial and lateral, both patellae were shortly afterward with a manipulation. Ten centered in the trochlea in the axial view, but years ago she had an arthroscopic synovec- there was narrowing with increased subchon- tomy. Four years ago she underwent right dral sclerosis of the medial patellofemoral arthroscopic medial meniscectomy, patellar joints. CT arthrography revealed loss of chondroplasty by arthroscopic shaving, and medial facet articular cartilage greater on the lateral release. There is constant pain that keeps showing increased anteversion bilaterally at her awake at night, pain walking, pain going 24° and 32° (Figure 21. Slight varus, inpointing of the femoral arthrosis after medial tibial tubercle patella (squinting), limited squatting, Motion transfer. In addition the tibias are being rotated R 0°–130°, L 0°–134°, L effusion, bilateral soft externally as a result of an external rotational tissue swelling, retropatellar crepitation, pull from a medially transferred tibial tubercle, increased lateral mobility bilaterally with and it is felt that the medial compartments apprehension on the right, not the left, were being overloaded by the increased medial increased medial mobility on the right, not the patellofemoral loading. There was no proof of 346 Clinical Cases Commented Figure 21. Doble contrast CT arthrogram showing loss medial patellofemoral cartilage bilaterally post-medial tibial tubercle transfer. The patient remains improved at was assumed that lateral patellar displacement 6 years post-osteotomy, although she has was responsible for the anterior knee pain and intermittent pain along the left medial joint it was assumed that a medial transfer of the tib- line that is felt to be due to an inadequate lat- ial tubercle would reduce this subluxation and eral transfer of the left tibial tubercle. It was assumed that lateral release, chon- droplasty, and medial meniscectomy would Case 5 improve the symptoms. A 33-year-old male hospital administra- made the situation worse. Lateral transfer of the tibial tuber- anterior knee pain of increased severity of cles and external rotational osteotomy of 3 months’ duration after a painful bucking Figure 21. CT rotational study showing bilateral femoral anteversion. Treatment was lateral tibial tubercle transfer to unload medial facet and intertrochanteric external rotational osteotomy to treat rotational alignment. Failure of Patellofemoral Surgery: Analysis of Clinical Cases 347 episode while in church. He complained of trochlear dysplasia, Achilles contracture, or the limping, recurrent swelling, locking, buckling patient’s height and weight. At age 20 (13 years earlier) and tibia, foot pronation, muscle contracture, he had realignment surgery (medial tubercle trochlear dysplasia, patellar height, and transfer, lnsall-type medial imbrication, and patellofemoral ligament laxity need to be con- lateral release) bilaterally. A simple lateral release or tibial tuber- had removal of loose bodies from the left knee. A 34-year-old female teacher was eral subluxation bilaterally and pain with referred for consultation regarding recurrent medial subluxation of the left patella, Q-angle dislocation of the patella starting at age 13. At 0°, medial facet tenderness bilaterally, increased age 30 because of pain and swelling she under- articular grind with side motion of the patella, went arthroscopy followed by medial transfer patella alta, 1+ laxity to varus stress bilaterally, of tibial tubercle (Elmslie-Trillat), lateral reti- thigh atrophy, Ober tight at 3 cm, prone hip nacular release, and chondroplasty. She now internal rotation 60°, external rotation 20°, tight presents with pain, swelling, weakness, and Achilles bilaterally. Patella alta, normal congruence eral foot hyperpronation, motion 0°–150°. CT arthrography revealed good quality Patella is hypermobile both to the medial and articular cartilage superiorly on the patella with the lateral direction. Gross atrophy of the marked loss of distal and especially medial quadriceps, moderate effusion, collateral and patellar articular cartilage; CT rotation study cruciate ligaments are stable, McMurray neg- revealed femoral anteversion 36° (normal 13°).
Thus order keflex 750mg line antibiotics omnicef, parental empowerment may be in competition with that of their children and with recommendations that carry professional authority buy discount keflex 500mg online antibiotics for uti zithromax; and the sense of partnership, which professionals strive to achieve, may suffer as a consequence. Again,the stepping order is downwards and with potential disagreements, siblings may find their needs, of all those being considered, the last to be realised. When parents are over protective of their children and professionals need to take decisions in the disabled child’s interest, parental and profes- sional opinion may exclude a view from the child involved. One explanation might be that communication difficulties and problems with the child’s expression of feelings might be cited for not including the child in the planning decision (Burke and Cigno 2001). My view is that it would be foolish not to recognise that parents may speak ably for their children, but it would be equally wrong not to make every effort to communicate in whatever way possible with the children themselves, and children include not only those with disabilities but 112 / BROTHERS AND SISTERS OF CHILDREN WITH DISABILITIES siblings too. It should not be a matter of competition either – of whose rights will be served; the rights of children should be in balance and equally considered, and when issues of child protection arise, the needs of the child come first. Summary In both research and practice, age and developmental factors are important. An adult, for example, has the duty and responsibility not to put a child or young person in a situation in which they cannot make informed decisions: a clear case is that of child sexual abuse, where the child cannot be said to give informed consent and where there is an imbalance of power and status. In a daily practice context, professionals must be careful about the way that they phrase questions, making knowledge of child development and language crucial to their work. Sinclair (1996) and Hill (1998) consider how to involve children in decision-making, stressing the need to listen to what they say about services. Although they are writing about children in general, their work has clear relevance for disabled children. Bond (1999) reviews a pack specifically designed for children with learning difficulties to help them communicate their wishes and participate in service design. She stresses the necessity for creative and child-friendly tools and environ- ments. Agencies like the National Childrens Bureau, SCOPE and Mencap may act as representatives of young disabled people. However, the possible exploitation of disabled people by professionals, researchers and non-disabled people needs to be fully considered; non-disabled profes- sionals should review the approach to their work that they adopt and be aware that the dissemination of information which concerns disabled people will affect those people’s lives (Connors and Stalker 2003, p. Nevertheless, it would be difficult to argue that siblings of children with disabilities do not need concerned adults to help them make their needs and wishes known (Ward 1998; Ward and Simons, 1998). It is part of parental and professional responsibility to speak up for children, but to do so at the cost of excluding the child’s viewpoint would essentially isolate the child further. SUPPORT SERVICES AND BEING EMPOWERED / 113 In the following case example, the experience of Rachel is compounded following a medical intervention which directs attention from her disabled sister, Susan, to herself. The sequence of events raises issues about possible causation which ultimately reflect on the difficulties which Rachel has to learn to handle. The case of Rachel and Susan (high negative association) Rachel, aged 14, has a younger sister Susan, aged 12, who has profound physical and intellectual disabilities. Susan attends a special school,requires one-to-one attention at all times and spends most of her time during the day in a purpose-built wheelchair. Susan is unable to feed herself and is fed via a tube directly into her stomach and, to add to her difficulties,she suffers from frequent epileptic fits. Rachel, a bright girl with a lively personality, attends a secondary school and helps with the care of Susan when at home. Rachel spoke only of caring for Susan; there was no expression equivalent to ‘playtime with Susan’, an indication that Rachel was more conscious of ‘a sense of duty to care’ (my expression) than simply enjoying the company of her sister. At the time of interview, Rachel had recovered from minor surgery to remove a lump from her neck, but some days after the operation she had experienced an ‘epileptic fit’ (as explained to her) which lasted about ten minutes. Rachel was taken to hospital and stayed for a period including overnight observation. She returned home only to find, some weeks later, that a similar thing happened again. The doctor indicated on the second occasion that the attack was likely to be of ‘psychological origins’ and not a true fit. Rachel was sent home and has had subsequent fits and experienced going to hospital on a regular basis as a consequence. Rachel has been prescribed medication to help control the fits,although an optimum balance appears yet to be determined and the fits continue on a regular basis. Comment The medical view appears to favour ‘psychological’ rather than a ‘physio- logical’ explanation for Rachel’s fits. Rachel indicates that she feels she is being blamed for something she cannot control.
The quality of life in acne: a comparison with general medical conditions using generic questionnaires purchase keflex 750mg fast delivery antibiotic dental abscess. Avaliac¸a˜o de Qualidade de Vida em Pacientes com Dermatoses: Estudo De Adap- tac¸a˜o e Validac¸a˜o da Dermatology Life Quality Index: (DLQI) para uma amostra Sul-Brasi- leira buy generic keflex 500 mg on line zinnat antibiotics for uti. Tese de Mestrado, Faculdade de Psicologia, Pontifıcia´ Universidade Catolica´ do Rio Grande do Sul, 2004. The effectiveness of massage treatment on cellulite as monitored by ultrasound imaging. Estudo histopatologico e histoquımico´ ´ de 100 casos. Impaired quality of adults with skin disease in primary care. Medication formulation affects quality of life: a randomized single-blind study of clobetasol propionate foam 0. PART I: DIAGNOSIS OF CELLULITE 2 Definition, Clinical Aspects, Associated Conditions, and Differential Diagnosis Doris Hexsel School of Medicine, University of Passo Fundo, Passo Fundo, Rio Grande do Sul, Brazil Taciana de Oliveira Dal’Forno Medical Sciences, Federal University of Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil Stela Cignachi School of Medicine, Lutheran University of Brazil (ULBRA) of Rio Grande do Sul, Canoas, Rio Grande do Sul, Brazil & DEFINITION ‘‘Cellulite’’ is a very common topographical alteration (1,2) in which the skin acquires an orange peel or mattress appearance (Fig. In this condition, alterations occur to the adipose tissue and microcirculation that result from blood and lymphatic disturbances causing fibrosclerosis of the connective tissue (2). It is considered a noninflammatory, degenerative phenomenon that provokes alterations to the hypodermis (5) producing irre- gular undulations on the skin overlying affected areas. Cellulite results from many complex events that involve the epidermis, dermis, and subcutaneous tissue (1). Anatomically, the cutaneous alterations found in cellulite are largely due to fibrosis of the connective tissues present in the dermis and/or in the subcutaneous tissue (7). DEFINITION, CLINICAL ASPECTS, ASSOCIATED CONDITIONS, AND DIFFERENTIAL DIAGNOSIS & 9 connective tissue of the reticular dermis is connected to the deep fascia by means of interlobular trabeculas (fibrous septum) from adipose tissue. Subcutaneous fat lobules are separated from one another by these thin, usually rigid strands of connective tissue that cross the fatty layer and connect the dermis to the underlying fascia. These strands stabilize the subcutis and divide the fat (8). The shortening of these septa due to fibrosis provokes retraction at the insertion points of the trabeculas (9), causing the depressions that are characteristic of cellulite. Nurnberger and Muller studied the anatomy and histology of fat and the connective¨ tissue structure of the subcutaneous tissue. They demonstrated, on anatomical bases, the characteristic mattress aspect of cellulite and pointed out the differences in the organiza- tion of the subcutaneous tissue between the two sexes (10,11). They also showed that in women the fibrous septa are usually orientated perpendicularly in relation to the cuta- neous surface, while in men they have a crisscross pattern (11). Several studies have shown that fat is divided into lobules, and that in women, these are larger and more rectangular when compared with those in men (4,11–15). These anatomical and histological findings explain the greater frequency of cellulite in women. In the same decade, Laguese described cellulite as a disease of the hypodermis, characterized by interstitial edema and an increase in fat (17). Initially, Curri defined cellulite as nodular liposclerosis (6,18) and later adopted the term ‘‘cellulitic dermohypodermosis’’ (19). In 1958, Merlen defined cellulite as a histoan- giopathy (20), and in 1978, Binazzi and Curri, after a histopathological study, suggested the term ‘‘sclerotic-fibrous-edematous panniculopathy’’ (21,22). Nurnberger and Muller¨ used the name ‘‘panniculosis of the dermis’’ (16,23) to describe cellulite from the histo- pathological viewpoint. Bacci and Leibaschoff suggest the use of the nomenclature ‘‘cellu- litic hypodermosis’’ (16). In recent years, the term ‘‘gynoid lipodystrophy’’ has been used in some studies (2,9,24). The terms ‘‘hydrolipodystrophy’’ and ‘‘herniation’’ of the fat with hypodermic tension bands are still in use for describing cellulite (25,26). The presence of the suffix ‘‘ite’’ in a medical term indicates inflammation; therefore, the term ‘‘cellulite’’ is more appropriately used to designate inflammation and/or infection of the subcutaneous tissue (27). However, the term ‘‘cellulite’’ has become very popular, and its use has been consecrated (20,28) by its being accepted throughout the world. Other synonyms often used for cellulite are listed in Table 1. There is evidence to suggest that estrogen is the element most probably involved in the initial dysfunction, aggravation, and persistence of cellulite (1,20,33).
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